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. 1,146 recalls have been distributed to Ohio in the last 12 months.
Showing 8841–8860 of 30,087 recalls
Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...
The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...
The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...
The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...
The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...
The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...
The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...
The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spiration Valve System (SVS) Valve in Cartridge -A one-way endobronchial...
The Issue: Mislabeled Patient Charge Label indicating model number SVS-V7-00 (7mm)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...
The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi and X 12-8 mm Conductive Cannula Reducer Recalled by Intuitive...
The Issue: Conductive Cannula Reducer metal tip may get dislodged from the plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME REVOLUTION RX 39-30-260-025 Material Number: M00584260 Recalled by...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM TRIVANTAGE EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due...
The Issue: There is potential for multiple issues due to a manufacturing nonconformity.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DREAMTOME 49-20MM/450CM Material Number: M00584020 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME REVOLUTION RX 39-20-450-025 Material Number: M00584250 Recalled by...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 39-20-260-025 Material Number: M00573080 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDRATOME RX 44-30MM/450CM Material Number: M00583070 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 39-30-260-025 Material Number: M00573100 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 44-20-450-035 Material Number: M00573050 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 44-30-450-035 Material Number: M00573070 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 39-30-450-025 Material Number: M00573110 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.