Product Recalls in Massachusetts
Product recalls affecting Massachusetts — including food, drugs, consumer products, medical devices, and vehicles distributed to Massachusetts. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,098 recalls have been distributed to Massachusetts in the last 12 months.
Showing 14541–14560 of 52,647 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: 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: 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: 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 RX 44-20-260-035 Material Number: M00573040 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 39-20-450-025 Material Number: M00573090 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 49-30-260-035 Material Number: M00573020 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 49-30-450-035 Material Number: M00573030 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: 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: Dreamtome RX Cannulating Sphincterotome-DREAMTOME 44-20MM/260CM Material...
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/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: Universal Chuck-The Universal Chuck is an Instrument Handle provided as...
The Issue: Top cap may loosen and detach if the Universal Chuck becomes jammed and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.