Product Recalls in Mississippi

Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,623 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,623 in last 12 months

Showing 85618580 of 28,172 recalls

Medical DeviceDecember 29, 2021· Stryker Leibinger GmbH & Co. KG

Recalled Item: MEDPOR Titan OFW - MTB - Right - 1.0mm Recalled by Stryker Leibinger GmbH &...

The Issue: Inside the packaging of one reported item a non-conforming product was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2021· Baxter Healthcare Corporation

Recalled Item: Baxter Spectrum IQ Infusion Pumps Recalled by Baxter Healthcare Corporation...

The Issue: There is the potential for reduced or non-delivery of medication, in some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 29, 2021· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)...

The Issue: There is the potential for reduced or non-delivery of medication, in some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2021· Hobbs Medical, Inc.

Recalled Item: Bronchial Microbiology Brush Recalled by Hobbs Medical, Inc. Due to The...

The Issue: The labeling for the Microbiology Brush identifies the device as a Bronchial...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· Intuitive Surgical, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· Hill-Rom, Inc.

Recalled Item: Liko Mobile Lifts: Primarily intended for use in nursing homes Recalled by...

The Issue: Missing bushing on Liko M220 and M230 causing wear and potential for patient...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· Hill-Rom, Inc.

Recalled Item: Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220...

The Issue: Missing bushing on Liko M220 and M230 causing wear and potential for patient...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

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.

Class II — Potential Health HazardOngoing