FDA Recalls, Food, Drug & Medical Device Alerts - Page 18 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.

Recall of Straumann Custom Abutment AS Ti Due to Manufacturing Mix-Up

FDA Recall of Embrace Drill Tower Due to Labeling Error

FDA Announces Recall of I.T.S. DUL and UOL Systems

Recall of Philips OMNI III TEE Ultrasound Transducer Announced

Recall of Philips Mini Multi TEE Ultrasound Transducer

Recall of Humeral Head Plate Devices by I.T.S. GmbH

Recall of DuraMax Chronic Hemodialysis Catheter Announced

I.T.S. GmbH Clavicula Plate Recall Over MRI Safety Concerns

Recall of Olympus Everest Bipolar Cutting Forceps Model 3005

Recall of TECNIS Eyhance IOL with Delivery System

I.T.S. GmbH Fibula Plate Recall

Recall of Straumann Custom Abutment Ti Devices

FDA Recall of Olympus Endoscope Air/Water Valve MAJ-1444

FDA Recall of Handy Solutions Neck & Shoulders Heating Pad

Recall of BioFlo DuraMax Catheters Due to Design Defect

Recall of Philips L17-5 Ultrasound Transducer for Labeling Clarification

I.T.S. LRS Locking System Recall Due to MRI Safety Concerns

Recall of Olympus Endoscope Reprocessor OER-Elite

FDA Recall of Tandem Insulin Pumps Due to User Guide Errors

Recall of Merit Medical's 16F Dual Valved Splittable Sheath Introducer

FDA Recall of Olympus PK Cutting Forceps Due to Welding Defect

Recall of Philips OMNI II TEE Ultrasound Transducer

FDA Announces Recall of Philips X3-1 Ultrasound Transducer

FDA Recall of Olympus Endoscope Reprocessor OER-Pro

Recall of Philips Respironics Trilogy Evo O2 Ventilator for Safety Issue

Recall of Imactis CT-Navigation System by GE Medical Systems

FDA Recall of Philips S4-1 Ultrasound Transducer

Recall of ProGuide Chronic Dialysis Catheters Due to Design Defect

Recall of Olympus Endoscope Suction Valve MAJ-1443

Recall of I.T.S. Pelvic Reconstruction System Over MRI Safety Concerns

I.T.S. Straight Plate Recall Due to MRI Safety Issues

FDA Recall of Flexible Cryoprobe by Erbe USA Inc

FDA Recall of CentrosFLO Hemodialysis Catheters Due to Design Defect

Recall of Distal Humeral Plates by I.T.S. GmbH

Recall of HLS Hand Locking Plates System by I.T.S. GmbH

Recall of Olympus PKS Cutting Forceps Due to Welding Defect

I.T.S. Screw System Recall Due to MRI Safety Concerns

Recall of Philips S5-2 Ultrasound Transducer Issued

FDA Recall of Olecranon Plates by I.T.S. GmbH

Recall of Flexible Cryoprobe by Erbe USA Inc

Recall of I.T.S. GmbH Foot Locking Plates and Hallux Osteotomy Plates

Recall of Philips Respironics Trilogy Evo Universal Ventilators

Recall of HCS Headless Compression Screw System by I.T.S. GmbH

FDA Recall of Orthalign Drill Plate Due to Manufacturing Issue

FDA Issues Recall for Orthalign Drill Plate Due to Manufacturing Defect

Recall of Pepsin 1:10,000 Powder Due to Potential Salmonella Contamination

FDA Recall of Bulk Packaged Colustrum Powder by Herbal Creations USA

Recall of King Harvest Sundried Tomato Hummus Due to Foreign Material

Recall of King Harvest Spinach Hummus Due to Foreign Material

Nuts.com Recalls Espresso Malted Milk Balls Over Undeclared Allergens