Product Recalls in Ohio
Product recalls affecting Ohio — including food, drugs, consumer products, medical devices, and vehicles distributed to Ohio. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,807 recalls have been distributed to Ohio in the last 12 months.
Showing 721–740 of 55,415 recalls
Recalled Item: Olympus Inner Sheath. Model No. A4741. for endoscopic diagnosis and Recalled...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Resection Inner Sheath for 26 Fr. Outer Sheath. Model Recalled by...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Resection Sheath. Model No. A2666T. for endoscopic diagnosis and...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic Recalled by...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Resection Sheath. Model No. A22014A and A22014T. for endoscopic...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Inner Sheath. Model No. A2642. for endoscopic diagnosis and Recalled...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Inner Sheath Recalled by Olympus Corporation of the Americas Due to...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Food to Live brand ORGANIC MORINGA LEAF POWDER Recalled by Lexunder Inc Due...
The Issue: Contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Food to Live brand ORGANIC SUPERGREENS POWDER MIX Recalled by Lexunder Inc...
The Issue: Contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Varenicline Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Sub...
The Issue: Sub potent drug: during the 9-month stability test conducted, the assay...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Halyard ORGAN RECOVERY OR PACK Recalled by AVID Medical, Inc. Due to Devices...
The Issue: Devices are not suitable for organ transplant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard ORGAN RECOVERY OR PACK Recalled by AVID Medical, Inc. Due to Devices...
The Issue: Devices are not suitable for organ transplant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard MINI PLUS KIT SOUTH Recalled by AVID Medical, Inc. Due to Devices...
The Issue: Devices are not suitable for organ transplant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEXLOCK Achilles Repair Implant Kits Recalled by Medline Industries, LP Due...
The Issue: There have been multiple complaints of drill bit fusing to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER DxH Diluent Recalled by Beckman Coulter, Inc. Due to Due to specific...
The Issue: Due to specific lots of diluents contributing to elevated platelet Daily...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ErgoStar CM 60 Recalled by Draeger, Inc. Due to Multiple complaints were...
The Issue: Multiple complaints were reported in which cracks formed in the hose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ErgoStar CM 45 Recalled by Draeger, Inc. Due to Multiple complaints were...
The Issue: Multiple complaints were reported in which cracks formed in the hose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ErgoStar CM 40 Model/Catalog Number: MP01840 Airway connector for conduction...
The Issue: Multiple complaints were reported in which cracks formed in the hose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.