Product Recalls in Illinois
Product recalls affecting Illinois — including food, drugs, consumer products, medical devices, and vehicles distributed to Illinois. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,137 recalls have been distributed to Illinois in the last 12 months.
Showing 14741–14760 of 55,304 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: 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: SonarMed AirWave Monitor Kit (Monitor Recalled by Covidien, LP Due to Prior...
The Issue: Prior to use on a patient, the device alarm speaker failed to annunciate on...
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.
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: JAGTOME RX 44-30-260-035 Material Number: M00573060 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.