Product Recalls in North Dakota
Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,036 recalls have been distributed to North Dakota in the last 12 months.
Showing 13361–13380 of 47,938 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: 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: 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: MIC* Percutaneous Endoscopic Gastrostomy PEG Kit - 20 Fr-PULL Recalled by...
The Issue: The External Retention Bolster contained in the kit may be a larger diameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX CHOLANGIOGRAM KIT Material Numbers: M00575241 M00575281 M00575321...
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: DREAMTOME 49-20MM/260CM Material Number: M00584000 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: DREAMTOME 49-30MM/450CM Material Number: M00584030 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: HYDRATOME RX 44-20MM/260CM Material Number: M00583040 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 49-20-260-035 Material Number: M00573000 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.