FDA Recalls - May 2026 (389 reports)
FDA Recalls issued during May 2026.
May 2026 ran 64% above the trailing 12-month average of 238 reports/month.
FDA Recalls
Katalyst Surgical Recalls DEX Ophthalmic Tissue Forceps
FDA ·
FDA Recalls high
Cook Beacon Tip Centimeter Sizing Catheter Recall
FDA ·
FDA Recalls
BioFire Spotfire Respiratory/Sore Throat Panel Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall
FDA ·
FDA Recalls
Mint Lesion Software Recall Due to Data Linking Issue
FDA ·
FDA Recalls high
Cook Aurous Centimeter Sizing Catheter Recall
FDA ·
FDA Recalls high
Intuitive 8 mm SureForm 30 Gray Reloads Recall
FDA ·
FDA Recalls
Medline KIT TRIPLE LUMEN INSERTION Recall Issued
FDA ·
FDA Recalls high
Cook Centimeter Sizing Catheter Recall
FDA ·
FDA Recalls
Erbe Medical Recalls ERBEFLO 2 Endoscopy Pump Tubing Sets
FDA ·
FDA Recalls
Erbe Medical Recalls ERBEFLO CleverCap Hybrid Tubing Sets
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Sterility Issue
FDA ·
FDA Recalls high
Halyard PERC TRAY Kit Recall Issued
FDA ·
FDA Recalls
Medline Convenience Kits Recall Issued for Sterility Assurance Issue
FDA ·
FDA Recalls
Medline KIT GENERAL CLOSURE Recall Issued
FDA ·
FDA Recalls
Medline Surgical Gowns Recall Issued Over Sterility Concerns
FDA ·
FDA Recalls
Medline Drape Pack-Choice Kits Recall Issued
FDA ·
FDA Recalls
Medline Convenience Kits Recall Issued for Sterility Concerns
FDA ·
FDA Recalls
Medline Convenience Kits Recall Issued
FDA ·
FDA Recalls
Medline Surgical Packs Recall Issued by FDA
FDA ·
FDA Recalls
Medline Convenience Kits Recall Issued by FDA
FDA ·
FDA Recalls
Medline Convenience Kits Recall for Sterility Assurance Issues
FDA ·
FDA Recalls
One Step UTI Test Recall Issued by FDA
FDA ·
FDA Recalls high
Halyard SAMMC ANGIOGRAPHY Kit Recall Issued
FDA ·
FDA Recalls
Katalyst Surgical DEX Ophthalmic Tissue Forceps Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Sterilization Issues
FDA ·
FDA Recalls high
Halyard HEART CATH SELF REGIONAL Kit Recall
FDA ·
FDA Recalls high
Halyard NEURO IR PERIPHERAL Kit Recall
FDA ·
FDA Recalls high
Halyard CATH LAB Kit Recall Issued
FDA ·
FDA Recalls
DFI One Step 10A In Vitro Diagnostic Test Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Sterility Concerns
FDA ·
FDA Recalls
Da Vinci X and Xi Surgical Systems Recall
FDA ·
FDA Recalls
Medline C-Section Kits Recall Due to Sterility Issues
FDA ·
FDA Recalls
BioCera Fibers Bone Void Filler Recall
FDA ·
FDA Recalls
Medline ADMIT KIT Recall Issued for Sterility Concerns
FDA ·
FDA Recalls
One Step pH Test Recall Issued by DFI Co., Ltd.
FDA ·
FDA Recalls
DFI One Step P In Vitro Diagnostic Test Recall
FDA ·
FDA Recalls high
Halyard CARDIAC CATH PACK Kits Recall Issued
FDA ·
FDA Recalls
QUCARE Total Cholesterol Test Recall Issued
FDA ·
FDA Recalls
ZENBONE Bone Void Filler Recall
FDA ·
FDA Recalls high
Halyard CATH LAB Kit Recall Issued by AVID Medical
FDA ·
FDA Recalls
Erbe Medical Recalls ERBEFLO CleverCap CO2 Tubing Sets
FDA ·
FDA Recalls
Medline Convenience Kits Recall Issued Over Sterility Concerns
FDA ·
FDA Recalls
Boston Scientific LUX-Dx II Plus Recall
FDA ·
FDA Recalls high
Halyard VA DETROIT CATH LAB PACK Kit Recall
FDA ·
FDA Recalls
Medline Surgical Drapes Recall Issued for Sterility Concerns
FDA ·
FDA Recalls
Boston Scientific LUX-DX II Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall for Sterility Issue
FDA ·
FDA Recalls
BioFire Joint Infection (JI) Panel Recall Issued
FDA ·
FDA Recalls
Centinel Spine Recalls Prodisc C SK Implant Due to Labeling Mix-Up
FDA ·
FDA Recalls
Medline Convenience Kits Recall Issued for Sterility Assurance Issues
FDA ·
FDA Recalls high
Halyard CARDIAC CATH PACK Recall Issued by AVID Medical
FDA ·
FDA Recalls
Medline Industries Recalls Surgical Procedure Kits
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Sterility Issues
FDA ·
FDA Recalls high
Ventec Life Systems Recalls VOCSN V+Pro Ventilators
FDA ·
FDA Recalls
DFI Uric Acid Test Recall Issued
FDA ·
FDA Recalls
Spacelabs Ultraview SL Command Module Recall
FDA ·
FDA Recalls high
Coronary Angio Pack Kits Recall Issued by American Contract Systems
FDA ·
FDA Recalls
Medline BASIC NERVE BLOCK TRAY W/LINEN Recall
FDA ·
FDA Recalls
Physio-Control LIFEPAK Defibrillators Recall
FDA ·
FDA Recalls
Centinel Spine Prodisc C SK Implant Recall for Labeling Mix-Up
FDA ·
FDA Recalls
One Step K In Vitro Diagnostic Test Recall Issued
FDA ·
FDA Recalls
Medline PPE Kit Recall Issued Over Sterility Assurance
FDA ·
FDA Recalls
Medline WMC I D PACK-LF Convenience Kits Recall
FDA ·
FDA Recalls high
Halyard CARDIAC CATH TRAY SHANDS JAX Kits Recall
FDA ·
FDA Recalls
Walker Honey Co Recalls Pecan Creamed Honey Products
FDA ·
FDA Recalls
Woodstock Organic Shelled Edamame Recall for Metal Pieces
FDA ·
FDA Recalls
Loard's Butterscotch Marble Ice Cream Recall
FDA ·
FDA Recalls
Loard's Blueberry Cheesecake Ice Cream Recall Issued
FDA ·
FDA Recalls
Christopher Ranch Peeled Garlic Recall Issued
FDA ·
FDA Recalls
Publix Bran Flakes Recall Issued for Foreign Material
FDA ·
FDA Recalls
Walker Honey Co Raspberry Creamed Honey Recall
FDA ·
FDA Recalls
Loard's Burgundy Cherry Ice Cream Recall Issued
FDA ·
FDA Recalls
Loard's Cookies and Cream Ice Cream Recall for Undeclared Allergens
FDA ·
FDA Recalls
Loard's Green Tea Ice Cream Recall for Undeclared Milk, Yellow #5
FDA ·
FDA Recalls
Loard's Raspberry Sherbert Recall for Undeclared Milk
FDA ·
FDA Recalls
Loard's Coffee Ice Cream Recall for Undeclared Milk
FDA ·
FDA Recalls
Loard's Mocha Chip Ice Cream Recall for Undeclared Milk
FDA ·
FDA Recalls high
Chick-fil-A Milk Wash Recall Due to Potential Salmonella
FDA ·
FDA Recalls
Loard's Black Walnut Ice Cream Recall
FDA ·
FDA Recalls
Loard's Strawberry Ice Cream Recall for Undeclared Milk, Red #40
FDA ·
FDA Recalls high
California Dairies Buttermilk Powder Recall
FDA ·
FDA Recalls
Loard's Chocolate Mint Ice Cream Recall
FDA ·
FDA Recalls
Loard's Horchata Ice Cream Recall for Undeclared Milk, Soy
FDA ·
FDA Recalls
Loard's Black Raspberry Ice Cream Recall Issued
FDA ·
FDA Recalls high
Raw Farm Original Raw Cheddar Recall
FDA ·
FDA Recalls
Loard's Butter Brickle Ice Cream Recall
FDA ·
FDA Recalls high
Raw Farm Raw Cheddar Jalapeno Recall
FDA ·
FDA Recalls
Loard's Maple Walnut Ice Cream Recall for Undeclared Allergens
FDA ·
FDA Recalls
Walker Honey Co Recalls Hatch Green Chile Creamed Honey
FDA ·
FDA Recalls
Loard's Black Raspberry Marble Ice Cream Recall Issued
FDA ·
FDA Recalls
Loard's Mango Ice Cream Recall for Undeclared Milk and Yellow #5
FDA ·
FDA Recalls
Loard's Toasted Almond Ice Cream Recall
FDA ·
FDA Recalls
Loard's Rainbow Sherbert Recall for Undeclared Allergens
FDA ·
FDA Recalls
Loard's Caramel Cashew Ice Cream Recall Issued
FDA ·
FDA Recalls
Loard's Vanilla Ice Cream Recall for Undeclared Milk
FDA ·
FDA Recalls
Loard's Mocha Almond Fudge Ice Cream Recall
FDA ·
FDA Recalls
Loard's Chocolate Ice Cream Recall for Undeclared Milk
FDA ·
FDA Recalls
Loard's Cherry Vanilla Ice Cream Recall Issued
FDA ·
FDA Recalls
Loard's Sea Salt Caramel Ice Cream Recall for Undeclared Allergens
FDA ·
FDA Recalls
Darkside of the Hive Creamed Honey Recall by Walker Honey Co
FDA ·
FDA Recalls
Montebianco Base Vegan Recall for Undeclared Milk Allergen
FDA ·
FDA Recalls
Loard's Pumpkin Ice Cream Recall for Undeclared Milk, Yellow #6
FDA ·
FDA Recalls
Loard's Orange Sherbert Recall for Undeclared Milk, Yellow #5
FDA ·
FDA Recalls
Loard's Chocolate Showers Ice Cream Recall Due to Undeclared Allergens
FDA ·
FDA Recalls
Loard's Rocky Road Ice Cream Recall for Undeclared Allergens
FDA ·
FDA Recalls
Target Recalls Good & Gather Sesame Teriyaki Chicken Over Undeclared Allergens
FDA ·
FDA Recalls
Loard's Egg Nog Ice Cream Recall for Undeclared Allergens
FDA ·
FDA Recalls
Loard's Pecan Praline Ice Cream Recall Issued
FDA ·
FDA Recalls
XZL Jelly Snacks Recall for Undeclared Dyes
FDA ·
FDA Recalls
Loard's Pistachio Ice Cream Recall Due to Undeclared Allergens
FDA ·
FDA Recalls
Walker Honey Co Recalls Cinnamon Creamed Honey
FDA ·
FDA Recalls high
Raw Farm Raw Cheddar Recall Amid E. coli Outbreak
FDA ·
FDA Recalls
Loard's Banana Ice Cream Recall for Undeclared Milk and Yellow #5
FDA ·
FDA Recalls
SunRidge Farms Organic Sunset Soup Mix Recall
FDA ·
FDA Recalls
Loard's Peanut Butter Fudge Ice Cream Recall
FDA ·
FDA Recalls high
Raw Farm Shredded Raw Cheddar Recall Over E. coli
FDA ·
FDA Recalls
Walker Honey Co Recalls Hatch Creamed Honey
FDA ·
FDA Recalls high
Griffith Foods Recalls Milk-N-Egg Mix Over Potential Salmonella
FDA ·
FDA Recalls
Loard's Coconut Pineapple Ice Cream Recall for Undeclared Milk
FDA ·
FDA Recalls
Loard's Chocolate Marble Ice Cream Recall for Undeclared Milk
FDA ·
FDA Recalls high
French Broad Chocolate Bette's Bake Sale Recall for Undeclared Walnut
FDA ·
FDA Recalls
SunRidge Farms Organic Black Beans Recall Issued
FDA ·
FDA Recalls
Loard's Almond Joy Ice Cream Recall for Undeclared Allergens
FDA ·
FDA Recalls
Walker Honey Co Blackberry Creamed Honey Recall
FDA ·
FDA Recalls
Walker Honey Co Lemon Creamed Honey Recall
FDA ·
FDA Recalls
Walker Honey Co Natural Creamed Honey Recall
FDA ·
FDA Recalls
Loard's Peppermint Ice Cream Recall for Undeclared Red #40
FDA ·
FDA Recalls
Garland Fresh Peeled Garlic Recall Issued by Tops Markets
FDA ·
FDA Recalls
Loard's Ube Ice Cream Recall Issued for Undeclared Ingredients
FDA ·
FDA Recalls
Loard's Lemon Chiffon Ice Cream Recall for Undeclared Allergens
FDA ·
FDA Recalls
Burgundy Cherry Ice Cream Recall Due to Undeclared Colors
FDA ·
FDA Recalls
Loard's Brownie Nut Fudge Ice Cream Recall Issued for Undeclared Allergens
FDA ·
FDA Recalls
Loard's Lime Sherbert Recall for Undeclared Allergens
FDA ·
FDA Recalls
Chocolate Showers Ice Cream Recall for Undeclared Soy
FDA ·
FDA Recalls
SunRidge Farms Organic Chili Bean Blend Recall
FDA ·
FDA Recalls high
Costco Meatloaf Seasoning Recall Over Salmonella Risk
FDA ·
FDA Recalls high
California Dairies Inc. Low Heat Non-Fat Dried Milk Powder Recall
FDA ·
FDA Recalls
Loard's Champagne Sherbert Recall for Undeclared Milk
FDA ·
FDA Recalls
Walker Honey Co Recalls Fain s Blackberry Honey Spread
FDA ·
FDA Recalls
Lundberg Family Farms White Rice Jasmine Recall
FDA ·
FDA Recalls
Horizon Organic Chocolate Milk Recall Issued
FDA ·
FDA Recalls high
Raw Farm Raw Cheddar Simply Shredded Cheese Recall
FDA ·
FDA Recalls high
California Dairies Inc. Recalls Non-Fat Dried Milk Powder
FDA ·
FDA Recalls
Loard's Peppermint Ice Cream Recall for Undeclared Allergens
FDA ·
FDA Recalls
Loard's Banana Ice Cream Recall for Undeclared Yellow #5
FDA ·
FDA Recalls
Ajanta Pharma Recalls Duloxetine Capsules
FDA ·
FDA Recalls
Fresenius DELFLEX Dialysis Solution Recall Due to Sterility Issue
FDA ·
FDA Recalls
Teva Recalls Octreotide Acetate Kits Over Sterility Concerns
FDA ·
FDA Recalls
DELFLEX Dialysis Solution Recall Due to Sterility Issue
FDA ·
FDA Recalls
Duloxetine Delayed-Release Capsules Recall
FDA ·
FDA Recalls
Buspirone Hydrochloride Tablets Recall Issued by Unichem
FDA ·
FDA Recalls
Duloxetine Delayed-Release Capsules Recall Issued
FDA ·
FDA Recalls
Enalapril Maleate Tablets Recall Due to Impurity Test Failure
FDA ·
FDA Recalls
Acella Naproxen Oral Suspension Recall
FDA ·
FDA Recalls
BD PurPrep Recall Due to Potential Sterility Issues
FDA ·
FDA Recalls
BD PurPrep Recall Issued by FDA
FDA ·
FDA Recalls
TPN Bag Recall Issued by Central Admixture Pharmacy Services
FDA ·
FDA Recalls
Philips SmartPath Device Recall for Stiffness Value Errors
FDA ·
FDA Recalls
Recall of Depuy Synthes ATTUNE Revision Hinge Femoral Device
FDA ·
FDA Recalls
Philips SmartPath Device Recall Over Potential Stiffness Errors
FDA ·
FDA Recalls
Recall of Philips MR 7700 Upgrade
FDA ·
FDA Recalls
Medline Medical Procedure Kits Recall
FDA ·
FDA Recalls
Zimmer Mixing Bowl and Spatula Recall Over Packaging Seal Issues
FDA ·
FDA Recalls
Recall of Medline Surgical ENT Prep Kits Due to Endotoxin Levels
FDA ·
FDA Recalls
Philips Ingenia Elition S Recall Due to Potential Errors
FDA ·
FDA Recalls
Recall of i-STAT EG6+ Cartridges by Abbott Point of Care Inc.
FDA ·
FDA Recalls
Recall of Depuy Synthes ATTUNE Revision Hinge Femoral Product
FDA ·
FDA Recalls
Medline EH Bronchoscopy Kit Recall
FDA ·
FDA Recalls
Recall of Philips Evolution Upgrade 1.5T Devices
FDA ·
FDA Recalls
Recall of Philips Bridge Prep Kit Due to Catheter Resistance Issue
FDA ·
FDA Recalls
FDA Recall of Centurion Dermatology Shave Kits
FDA ·
FDA Recalls
Recall of Centurion Medical Kits by Medline Industries
FDA ·
FDA Recalls
Recall of Philips Achieva 3.0T Device
FDA ·
FDA Recalls
FDA Recall of Philips Bridge Prep Kit Due to Catheter Resistance
FDA ·
FDA Recalls
Recall of BD GasPak EZ Campy Pouch System for Low CO2 Levels
FDA ·
FDA Recalls
Siemens epoc BGEM BUN Test Card Recall Due to Inaccurate Results
FDA ·
FDA Recalls
FDA Recall of Abbott i-STAT EG7+ Cartridges Due to Inaccurate Test Results
FDA ·
FDA Recalls
Recall of Immy Myco DDR Trident Neutralization Buffer Due to Contaminants
FDA ·
FDA Recalls
FDA Recall of Healthmark Tip Protectors Due to Lack of Clearance
FDA ·
FDA Recalls
Philips MR 7700 Device Recall Announced
FDA ·
FDA Recalls
Philips Ingenia 1.5T Devices Recall Over Stiffness Value Errors
FDA ·
FDA Recalls
Recall of Philips Achieva 1.5T Medical Device
FDA ·
FDA Recalls
Recall of Philips Ingenia 3.0T CX Devices
FDA ·
FDA Recalls high
WHILL Model F Wheelchair Recall Due to Cyber Vulnerability
FDA ·
FDA Recalls
Recall of Advanced Bionics HiResolution Bionic Ear System Battery Pak
FDA ·
FDA Recalls
Recall of Philips Ingenia Elition X Devices
FDA ·
FDA Recalls high
FDA Recall of AIDBAGs First Aid Kits by North American Rescue LLC.
FDA ·
FDA Recalls
Recall of Philips Ingenia 1.5T CX Medical Device
FDA ·
FDA Recalls
Recall of Philips Achieva 1.5T Devices Due to Potential Errors
FDA ·
FDA Recalls
Medline Recalls Medical Procedure Kits Due to Endotoxin Levels
FDA ·
FDA Recalls
Recall of Straumann n!ce PMMA Full-arch Restoration
FDA ·
FDA Recalls
Recall of Philips Ingenia Ambition S Devices
FDA ·
FDA Recalls
Medline Medical Procedure Kits Recall Over Endotoxin Levels
FDA ·
FDA Recalls
FDA Announces Recall of Leksell Vantage Arc System
FDA ·
FDA Recalls
Recall of Medline PEDS AIRWAY PACK Kits Due to Endotoxin Levels
FDA ·
FDA Recalls
Recall of i-STAT G3+ Cartridges by Abbott
FDA ·
FDA Recalls
Medline Recalls Medical Procedure Kits Over Endotoxin Levels
FDA ·
FDA Recalls
Philips Evolution Upgrade 3.0T Recall for Stiffness Value Errors
FDA ·
FDA Recalls
Recall of Medline Centurion Medical Kits Due to Non-Sterile Alcohol Prep Pads
FDA ·
FDA Recalls
Straumann n!ce Zr Dental Implant Abutments Recall
FDA ·
FDA Recalls
Recall of Medline Medical Kits Containing Non-Sterile Alcohol Prep Pads
FDA ·
FDA Recalls
FDA Recall of Siemens Dimension Creatinine Flex Reagent Cartridge
FDA ·
FDA Recalls high
Boston Scientific Pacemaker Recall for Software Update
FDA ·
FDA Recalls
Philips Ingenia 3.0T Device Recall Announced
FDA ·
FDA Recalls
Medline Cervical Pack Recall Due to Endotoxin Levels
FDA ·
FDA Recalls
Medline Spinal Fusion Kit Recall
FDA ·
FDA Recalls
Recall of VACUUM BAG SU LARGE Specimen Container by Milestone S.R.L.
FDA ·
FDA Recalls
Medline Medical Kits Recall Due to Non-Sterile Alcohol Prep Pads
FDA ·
FDA Recalls
Medline Robotic Hysterectomy Kits Recall Over Endotoxin Levels
FDA ·
FDA Recalls
Recall of Philips SmartPath to Ingenia Elition X Devices
FDA ·
FDA Recalls
Medline Kits Recall Due to Non-Sterile Alcohol Prep Pads
FDA ·
FDA Recalls
Recall of Medline Microdiscectomy Packs Due to Endotoxin Levels
FDA ·
FDA Recalls
Medline ANGIO PACK-LF Recall Over Endotoxin Levels
FDA ·
FDA Recalls
Medline SPINE PACK-LF Kit Recall
FDA ·
FDA Recalls high
WHILL Model C2 Wheelchair Recall Over Cyber Vulnerability
FDA ·
FDA Recalls
FDA Recall of Medline Medical Kits Due to Non-Sterile Alcohol Prep Pads
FDA ·
FDA Recalls high
Boston Scientific CRT Devices Recall
FDA ·
FDA Recalls
Recall of Philips SmartPath to dStream Device
FDA ·
FDA Recalls
FDA Recall of Genius Review Station Display
FDA ·
FDA Recalls
Recall of BD GasPak EZ CO2 Pouch System Due to Low Carbon Dioxide Levels
FDA ·
FDA Recalls high
Enoki Mushroom Recall by HEMU TRADING INC
FDA ·
FDA Recalls
Recall of KLG Kesar Mukhwas by Ganesha Enterprises
FDA ·
FDA Recalls
Recall of Calypso Tropic Tango Lemonade Due to Undeclared Yellow No. 5
FDA ·
FDA Recalls
FDA Recall of My Mochi Strawberry Non-Dairy Frozen Dessert Due to Foreign Object
FDA ·
FDA Recalls
Recall of 52USA Popping Boba Strawberry Flavor
FDA ·
FDA Recalls
Recall of Einstein Bros. Bagels Honey Almond Shmear Due to Undeclared Allergen
FDA ·
FDA Recalls
Recall of Specially SELECTED Vanilla Creme Brulee Due to Possible Glass Contamination
FDA ·
FDA Recalls
FDA Recall of 52USA Popping Boba Mango Flavor Over Unapproved Colors
FDA ·
FDA Recalls
FDA Recall of 52USA Popping Boba Due to Unapproved Colors
FDA ·
FDA Recalls
FDA Recall of Negita Cracker- Shrimp Due to Undeclared Ingredient
FDA ·
FDA Recalls
Recall of fentaNYL Citrate Injectable Solution by Wells Pharma
FDA ·
FDA Recalls
Recall of Levocarnitine Injection by American Regent
FDA ·
FDA Recalls
FDA Recall of Phenylephrine Hydrochloride Injectable Solution by Wells Pharma
FDA ·
FDA Recalls
Systane Eye Gel Recall Due to Sterility Concerns
FDA ·
FDA Recalls
FDA Recall of Lidocaine Wound Gel Due to Failed pH Specifications
FDA ·
FDA Recalls
FDA Recall of fentaNYL Citrate Injectable Solution by Wells Pharma
FDA ·
FDA Recalls
FDA Recall of Optase Dry Eye Intense Drops Due to Sterility Concerns
FDA ·
FDA Recalls
Recall of Alendronate Sodium Oral Solution by Hikma Pharmaceuticals
FDA ·
FDA Recalls
GenTeal Tears Eye Gel Recall Due to Sterility Concerns
FDA ·
FDA Recalls
iVIZIA Dry Eye Recall Over Sterility Issues
FDA ·
FDA Recalls
Recall of Ketamine Hydrochloride Injectable Solution by Wells Pharma
FDA ·
FDA Recalls
Recall of Similasan iVIZIA Sterile Lubricant Eye Drops
FDA ·
FDA Recalls
Recall of Medline Convenience Kits Due to Unapproved Design Changes
FDA ·
FDA Recalls
Recall of Arrowg+ard Blue MAC Two-Lumen Central Venous Access Kit
FDA ·
FDA Recalls
Recall of Custom Convenience Kits Pre Op Kit - NS
FDA ·
FDA Recalls
Recall of Olympus OER-ELITE Endoscope Reprocessor Connecting Tubes
FDA ·
FDA Recalls
Recall of Arrow Echogenic Introducer Needle Due to Manufacturing Issue
FDA ·
FDA Recalls
Recall of AccuVu Angiographic Catheter Issued
FDA ·
FDA Recalls
Recall of Soft-Vu Angiographic Catheter by Angiodynamics
FDA ·
FDA Recalls
FDA Recall of Medline PICC TRAY Devices
FDA ·
FDA Recalls high
Uvlizer Handheld UV-C Germicidal Wand Recall
FDA ·
FDA Recalls
Recall of Flamingo Funnel Large by SurgiSmoke Solutions
FDA ·
FDA Recalls
Recall of Diversatek Healthcare Viper 3-Stage Balloon Dilator
FDA ·
FDA Recalls
Recall of Diversatek Healthcare Viper 3-Stage Wire Guided Balloon Dilator
FDA ·
FDA Recalls
FDA Mandated Recall of Uvlizer Handheld UV-C Germicidal Wand
FDA ·
FDA Recalls
Recall of OER-ELITE Endoscope Reprocessor Connecting Tubes
FDA ·
FDA Recalls
FDA Recall of LSL Healthcare Infant Central Line Dressing Change Kit
FDA ·
FDA Recalls
Medline Control Syringes Recall Over Rescinded Regulatory Clearances
FDA ·
FDA Recalls
Recall of Olympus Thunderbeat II Shears Due to Detachment Risk
FDA ·
FDA Recalls
FDA Recall of Olympus OER-ELITE Endoscope Reprocessor Connecting Tubes
FDA ·
FDA Recalls
FDA Recall of Medline Convenience Kits Due to Unapproved Design Changes
FDA ·
FDA Recalls
Medline Syringe Kits Recall for Unapproved Design Changes
FDA ·
FDA Recalls
Recall of Medline GYN Laparoscopy Pack
FDA ·
FDA Recalls
FDA Recalls Medline Syringes Due to Regulatory Issues
FDA ·
FDA Recalls
Medline Industries LP Recall of Medical Devices
FDA ·
FDA Recalls
FDA Recalls Medline Medical Kits Due to Regulatory Issues
FDA ·
FDA Recalls
FDA Recall of Olympus Thunderbeat II Shears for Potential Detachment
FDA ·
FDA Recalls
FDA Recall of Medline ARTHROSCOPY PACK Due to Regulatory Clearance Issues
FDA ·
FDA Recalls
FDA Recall of Angiodynamics Soft-Vu Angiographic Catheter Due to Manufacturing Defect
FDA ·
FDA Recalls
FDA Recall of Arrowg+ard Blue Plus Four-Lumen CVC Kits
FDA ·
FDA Recalls
Recall of LSL Healthcare IV Start Kit
FDA ·
FDA Recalls
FDA Recall of AccuVu Angiographic Catheter Due to Manufacturing Defect
FDA ·
FDA Recalls
FDA Recall of Avitene Ultrafoam Hemostat Due to Potential Contamination
FDA ·
FDA Recalls
FDA Recall of Flamingo Funnel Medium by SurgiSmoke Solutions
FDA ·
FDA Recalls
Recall of LSL Healthcare Central Line Dressing Kit
FDA ·
FDA Recalls
Recall of Medline GENERAL LAPAROSCOPY Kits
FDA ·
FDA Recalls
Medline Industries Recalls Medical Devices Due to Regulatory Issues
FDA ·
FDA Recalls
Recall of LSL Healthcare Standard Central Line Dressing Change Kit
FDA ·
FDA Recalls
FDA Recall of Custom Convenience Kits Pre Op Kit - NS
FDA ·
FDA Recalls
Recall of Medline Convenience Kits Due to Design Changes
FDA ·
FDA Recalls
FDA Recall of OER-ELITE Endoscope Reprocessor Connecting Tubes
FDA ·
FDA Recalls
Recall of Medline DYNJ44813D Kits
FDA ·
FDA Recalls
FDA Recall of LeadCare Ultra Blood Lead Test Kit
FDA ·
FDA Recalls
Recall of Percutaneous Sheath Introducer by Arrow International
FDA ·
FDA Recalls
Recall of Soft-Vu Angiographic Catheter Due to Manufacturing Defect
FDA ·
FDA Recalls
FDA Recall of FLEXTIP PLUS Epidural Catheter Announced
FDA ·
FDA Recalls
FDA Recall of Soft-Vu Angiographic Catheter by Angiodynamics
FDA ·
FDA Recalls
FDA Recall of FoundationOneCDx Software by Foundation Medicine
FDA ·
FDA Recalls
Medline Convenience Kits Recall for Unapproved Design Changes
FDA ·
FDA Recalls
Recall of Soft-Vu Angiographic Catheter by Angiodynamics, Inc.
FDA ·
FDA Recalls
Recall of Medline Breast Pack Kits Due to Regulatory Clearance Issues
FDA ·
FDA Recalls
Medline Namic Syringes Recall Over Regulatory Issues
FDA ·
FDA Recalls
Recall of ARROW Pressure Injectable Central Venous Catheters
FDA ·
FDA Recalls
Recall of ARROW Radial Artery Catheterization Kits Due to Manufacturing Issue
FDA ·
FDA Recalls
FDA Issues Recall for Soft-Vu Angiographic Catheter Due to Manufacturing Defect
FDA ·
FDA Recalls
Recall of Access Total T4 Calibrator by Beckman Coulter Due to Accuracy Issues
FDA ·
FDA Recalls
FDA Recall of LeadCare II Blood Lead Test Kits
FDA ·
FDA Recalls
Medline Convenience Kits Recall Over Unapproved Design Changes
FDA ·
FDA Recalls
Recall of Rover Mobile X-ray System Due to Potential Malfunction
FDA ·
FDA Recalls
Medline Industries Recalls Medical Devices Over Regulatory Issues
FDA ·
FDA Recalls
Recall of Flamingo Funnel Small by SurgiSmoke Solutions
FDA ·
FDA Recalls
Medline Industries Recalls Medical Kits Over Regulatory Clearance Issues
FDA ·
FDA Recalls
Recall of Medline Hysteroscopy Pack and Sling Pack
FDA ·
FDA Recalls
Recall of Magellan Diagnostics' LeadCare Plus Blood Lead Test Kit
FDA ·
FDA Recalls
FDA Recall of Angiodynamics' AccuVu Angiographic Catheter Due to Manufacturing Defect
FDA ·
FDA Recalls
Recall of MAC Two-Lumen Central Venous Access Kit
FDA ·
FDA Recalls
FDA Announces Recall of Olympus Thunderbeat II Shears
FDA ·
FDA Recalls
Recall of LSL Healthcare Foley Urine Collection Kit
FDA ·
FDA Recalls
Medline Kits Recall Due to Rescinded Regulatory Clearances
FDA ·
FDA Recalls
Medline Industries Recall of Medical Device Kits
FDA ·
FDA Recalls
LSL Healthcare Wound Closure Tray Recall
FDA ·
FDA Recalls
Recall of AccuVu Angiographic Catheter by Angiodynamics
FDA ·
FDA Recalls
FDA Recall of Medline Namic Guidewires
FDA ·
FDA Recalls
Recall of Olympus Thunderbeat II Shears Due to Potential Detachment Risk
FDA ·
FDA Recalls
FDA Announces Recall of Medline Convenience Kits with Syringes
FDA ·
FDA Recalls
Recall of Medline Convenience Kits with 10mL Syringes Due to Unapproved Design Changes
FDA ·
FDA Recalls
Recall of Medline Heart Transplant Biopsy Kits
FDA ·
FDA Recalls
CHIPS AHOY! Baked Bites Brookie Recall Due to Hard Corn Starch Lumps
FDA ·
FDA Recalls
Recall of EL MEXICANO Horchata Drink Due to Undeclared Milk
FDA ·
FDA Recalls
Recall of EL MEXICANO Instant Horchata Drink Due to Undeclared Milk
FDA ·
FDA Recalls high
FDA Recall of SALUTE SEASONINGS Ground All Spice Due to Salmonella Risk
FDA ·
FDA Recalls
Recall of Bulk Horchata Powder Due to Undeclared Milk
FDA ·
FDA Recalls
FDA Recall of Bombay Kitchen Punjabi Mix Due to Undeclared Colors
FDA ·
FDA Recalls
Summit Import Corporation Recalls Spice Powder Over High Lead Levels
FDA ·
FDA Recalls high
Kirkland Signature Traditional Madeleines Recall
FDA ·
FDA Recalls
FDA Recalls Bombay Kitchen Tikka Sev for Undeclared Colors
FDA ·
FDA Recalls
Recall of Pantoprazole Sodium Tablets Due to Discoloration
FDA ·
FDA Recalls
Recall of Premier Monsel's Solution Due to Labeling Error
FDA ·
FDA Recalls
Furosemide Tablets Recall by Leading Pharma
FDA ·
FDA Recalls
Recall of Omega-3-Acid Ethyl Esters Capsules
FDA ·
FDA Recalls high
FDA Issues Recall for B Braun Hemodialysis Bloodlines
FDA ·
FDA Recalls high
Recall of B. Braun Hemodialysis Bloodlines Due to Air Bubble Risk
FDA ·
FDA Recalls
FDA Recall of Cytal Wound Matrix Due to Endotoxin Issues
FDA ·
FDA Recalls
LinkBio CORE Workstation Recall Over Display Error
FDA ·
FDA Recalls
Recall of Cytal Burn Matrix 7x10 cm by Integra LifeSciences
FDA ·
FDA Recalls high
Recall of B. Braun Hemodialysis Bloodlines Due to Potential Air Bubble Risk
FDA ·
FDA Recalls
Recall of CENTURION Circumcision Kit by Medline Industries
FDA ·
FDA Recalls
Siemens ARTIS Pheno Devices Recall
FDA ·
FDA Recalls
Recall of Philips Spectral CT on Rails Systems Due to Software Issues
FDA ·
FDA Recalls
Recall of Cytal Wound Matrix 2-Layer Issued by Integra LifeSciences
FDA ·
FDA Recalls
Recall of Elegance Anterior Cervical Plates by Clariance-SAS
FDA ·
FDA Recalls high
FDA Recall of iLet Ace Pump Kit and Software
FDA ·
FDA Recalls
Philips AneurysmFlow Device Recall Due to Safety Issue
FDA ·
FDA Recalls
Recall of Cellex Photopheresis System Kits
FDA ·
FDA Recalls
FDA Recall of Instinct Plus Endoscopic Clipping Device
FDA ·
FDA Recalls
FDA Recall of Cytal Burn Matrix by Integra LifeSciences
FDA ·
FDA Recalls
Recall of Gentuity HF-OCT Imaging System for Potential Measurement Issues
FDA ·
FDA Recalls
Yeastone Broth Recall by Remel, Inc.
FDA ·
FDA Recalls high
Recall of Omnipod 5 Pods Due to Manufacturing Defect
FDA ·
FDA Recalls high
FDA Recall of Arjo Tenor Mobile Passive Patient Lift
FDA ·
FDA Recalls
Recall of React Health PHOENIX 5L Oxygen Concentrator
FDA ·
FDA Recalls
Recall of Bee Well Wildflower Honey Due to High Sugar Content
FDA ·
FDA Recalls
Recall of Booey's Dragon's Breath Sauce Due to Allergen Labeling Issue
FDA ·
FDA Recalls
Recall of Quality Choice Cough Drops Over Quality Concerns
FDA ·
FDA Recalls
FDA Announces Recall of MGC Health Cough Drops
FDA ·
FDA Recalls
Recall of Blemish Spot Treatment Due to Stability Issues
FDA ·
FDA Recalls
FDA Recall of HydroPeptide Clear Alliance Serum Due to Benzene Contamination
FDA ·
FDA Recalls
Quality Choice Menthol Cough Drops Recall
FDA ·
FDA Recalls
Recall of Magnesium Chloride by Avantor Performance Materials LLC
FDA ·
FDA Recalls
Recall of Cinacalcet Hydrochloride Tablets by Cipla USA Inc.
FDA ·
FDA Recalls
Hydrocortisone Balm Recall by Island Kinetics
FDA ·
FDA Recalls
Desmopressin Acetate Nasal Spray Recall
FDA ·
FDA Recalls
Recall of Caring Mill Cough Drops Announced
FDA ·
FDA Recalls
Recall of SLMD Benzoyl Peroxide Acne Lotion Due to Chemical Contamination
FDA ·
FDA Recalls
Recall of Quality Choice Cough Drops Vanilla Honey Due to Quality Concerns
FDA ·
FDA Recalls
Menthol Flavor Cough Drop Recall Announced by FDA
FDA ·
FDA Recalls
Recall of Quality Choice Cough Drops Creamy Strawberry
FDA ·
FDA Recalls
Recall of QUALITY CHOICE Cough Drops Due to Quality Concerns
FDA ·
FDA Recalls
FDA Recall of Memantine Hydrochloride Extended-Release Capsules
FDA ·
FDA Recalls
FDA Recall of Quality Choice Honey Lemon Cough Drops
FDA ·
FDA Recalls
Fluocinonide Cream Recall by FDA
FDA ·
FDA Recalls
Recall of Discount Drug Mart Cough Drops
FDA ·
FDA Recalls
FDA Recall of Albuterol Sulfate Inhalation Solution Due to Illegible Labels
FDA ·
FDA Recalls
Recall of Quality Choice Honey Lemon Sugar-Free Cough Drops
FDA ·
FDA Recalls
Recall of Cinacalcet Hydrochloride Tablets by Cipla USA
FDA ·
FDA Recalls
Fluocinonide Cream Recall by Sun Pharmaceutical
FDA ·
FDA Recalls
FDA Recall of Essential Calming Skin Gel Due to Subpotency
FDA ·
FDA Recalls
Recall of SLMD BP Acne Spot Treatment Due to Benzene Contamination
FDA ·
FDA Recalls high
FDA Recall of Epinephrine Injection Over Sterility Concerns
FDA ·
FDA Recalls
FDA Recall of Cipla's Cinacalcet Hydrochloride Tablets
FDA ·
FDA Recalls
FDA Recall of Semaglutide-Glycine-Cyanocobalamin Injectable Due to Sterility Concerns
FDA ·
FDA Recalls
Remedy Gel Recall: FDA Issues Alert for Subpotent Drug
FDA ·
FDA Recalls
Recall of Honey Lemon Flavor Cough Drops Announced
FDA ·
FDA Recalls
FDA Recall of Discount Drug Mart Menthol Cough Drops
FDA ·
FDA Recalls
Recall of MGC Health Cough Drops Announced
FDA ·
FDA Recalls
FDA Recall of FHF Farmhouse Fresh Midnight Clearing Night Lotion Due to Benzene Contamination
FDA ·
FDA Recalls
Recall of MGC Health Honey Lemon Cough Drops
FDA ·
FDA Recalls
FDA Recall of Fluocinonide Cream Over Viscosity Issues
FDA ·
All federal data sources used on this page
- FDA Enforcement Report - official FDA recall classifications for food, drugs, devices, biologics, and tobacco. fda.gov/safety/recalls
- FDA Recalls, Withdrawals & Safety Alerts API - openFDA recall endpoint. open.fda.gov
- USDA Food Safety and Inspection Service (FSIS) - meat, poultry, and processed-egg-product recalls. fsis.usda.gov/recalls
- CDC Foodborne Outbreaks - outbreak investigation context for food recalls. cdc.gov/foodsafety/outbreaks
- Consumer Product Safety Commission (CPSC) - non-food consumer-product recalls cross-reference. cpsc.gov/recalls
- NHTSA Vehicle Recalls - automobile and tire recalls cross-reference. nhtsa.gov/recalls