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 701–720 of 30,087 recalls
Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFire Respiratory Panel 2.1 Recalled by BioFire Diagnostics, LLC Due to...
The Issue: Due to unintended movement of pouch chemistry, nucleic acid test may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareLink Clinic Recalled by Medtronic MiniMed, Inc. Due to Software error...
The Issue: Software error causing incorrect data to be displayed on the 24-hour Sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow PRUTest Platelet Reactivity Test UDI-DI code: 10711234150078...
The Issue: Due to an device without a premarket clearance being incorrectly package and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System....
The Issue: Potential for anesthesia leakage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Isoflurane (ISO) V90 Electronic Vaporizer with the A9 Anesthesia System....
The Issue: Potential for anesthesia leakage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HR-ACT (High Range Activated Clotting Time Cartridges) Recalled by...
The Issue: Medtronic personnel observed trace amounts of dry blood on the external...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MONARCH Bronchoscope. Model Number: MBR-000211-B Recalled by Auris Health,...
The Issue: Potential that product was leak tested with equipment outside of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emdogain Recalled by Straumann USA LLC Due to The possibility for this...
The Issue: The possibility for this product that is intended for demonstration purposes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.