FDA Recalls, Food, Drug & Medical Device Alerts - Page 10 of 27

Latest food, drug, and medical device recalls issued by the U.S. Food and Drug Administration. Class I, II, and III recall classifications, affected products, and consumer guidance.

Philips Ingenia 3.0T Device Recall Announced

Medline Cervical Pack Recall Due to Endotoxin Levels

Medline Spinal Fusion Kit Recall

Recall of VACUUM BAG SU LARGE Specimen Container by Milestone S.R.L.

Medline Medical Kits Recall Due to Non-Sterile Alcohol Prep Pads

Medline Robotic Hysterectomy Kits Recall Over Endotoxin Levels

Recall of Philips SmartPath to Ingenia Elition X Devices

Medline Kits Recall Due to Non-Sterile Alcohol Prep Pads

Recall of Medline Microdiscectomy Packs Due to Endotoxin Levels

Medline ANGIO PACK-LF Recall Over Endotoxin Levels

Medline SPINE PACK-LF Kit Recall

WHILL Model C2 Wheelchair Recall Over Cyber Vulnerability

FDA Recall of Medline Medical Kits Due to Non-Sterile Alcohol Prep Pads

Boston Scientific CRT Devices Recall

Recall of Philips SmartPath to dStream Device

FDA Recall of Genius Review Station Display

Recall of BD GasPak EZ CO2 Pouch System Due to Low Carbon Dioxide Levels

Enoki Mushroom Recall by HEMU TRADING INC

Recall of KLG Kesar Mukhwas by Ganesha Enterprises

Recall of Calypso Tropic Tango Lemonade Due to Undeclared Yellow No. 5

FDA Recall of My Mochi Strawberry Non-Dairy Frozen Dessert Due to Foreign Object

Recall of 52USA Popping Boba Strawberry Flavor

Recall of Einstein Bros. Bagels Honey Almond Shmear Due to Undeclared Allergen

Recall of Specially SELECTED Vanilla Creme Brulee Due to Possible Glass Contamination

FDA Recall of 52USA Popping Boba Mango Flavor Over Unapproved Colors

FDA Recall of 52USA Popping Boba Due to Unapproved Colors

FDA Recall of Negita Cracker- Shrimp Due to Undeclared Ingredient

Recall of fentaNYL Citrate Injectable Solution by Wells Pharma

Recall of Levocarnitine Injection by American Regent

FDA Recall of Phenylephrine Hydrochloride Injectable Solution by Wells Pharma

Systane Eye Gel Recall Due to Sterility Concerns

FDA Recall of Lidocaine Wound Gel Due to Failed pH Specifications

FDA Recall of fentaNYL Citrate Injectable Solution by Wells Pharma

FDA Recall of Optase Dry Eye Intense Drops Due to Sterility Concerns

Recall of Alendronate Sodium Oral Solution by Hikma Pharmaceuticals

GenTeal Tears Eye Gel Recall Due to Sterility Concerns

iVIZIA Dry Eye Recall Over Sterility Issues

Recall of Ketamine Hydrochloride Injectable Solution by Wells Pharma

Recall of Similasan iVIZIA Sterile Lubricant Eye Drops

Recall of Medline Convenience Kits Due to Unapproved Design Changes

Recall of Arrowg+ard Blue MAC Two-Lumen Central Venous Access Kit

Recall of Custom Convenience Kits Pre Op Kit - NS

Recall of Olympus OER-ELITE Endoscope Reprocessor Connecting Tubes

Recall of Arrow Echogenic Introducer Needle Due to Manufacturing Issue

Recall of AccuVu Angiographic Catheter Issued

Recall of Soft-Vu Angiographic Catheter by Angiodynamics

FDA Recall of Medline PICC TRAY Devices

Uvlizer Handheld UV-C Germicidal Wand Recall

Recall of Flamingo Funnel Large by SurgiSmoke Solutions

Recall of Diversatek Healthcare Viper 3-Stage Balloon Dilator