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. 2,635 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,635 in last 12 months

Showing 54415460 of 28,172 recalls

Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: AT HOME MARIJUANA TEST STRIP Recalled by Family Dollar Stores, Llc. Due to...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: FIXODENT ORG CREAM 2.4OZ Recalled by Family Dollar Stores, Llc. Due to...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: VERIQUICK PREGNANCY TEST 1CT Recalled by Family Dollar Stores, Llc. Due to...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Baxter Healthcare Corporation

Recalled Item: HILLROM PROGRESSA+ BED Recalled by Baxter Healthcare Corporation Due to...

The Issue: Progressa+ beds have the potential for static buildup from the casters...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2023· Roche Diagnostics Operations, Inc.

Recalled Item: Tina-quant D-Dimer Test System Recalled by Roche Diagnostics Operations,...

The Issue: Elevated results were detected with Li-heparin plasma samples when compared...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Edge Biologicals Inc

Recalled Item: Edge Biologicals STERILE WATER Recalled by Edge Biologicals Inc Due to Due...

The Issue: Due to product outer packaging incorrectly labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Carestream Health, Inc.

Recalled Item: DRX Revolution Mobile X-Ray System Recalled by Carestream Health, Inc. Due...

The Issue: Unexpected failure of electrical components within the CPI generator.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Stanbio Laboratory, LP

Recalled Item: STAT-Site M BHB Test Strips Recalled by Stanbio Laboratory, LP Due to...

The Issue: Deterioration in the stability of the Test Strips results in diminished...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA III Gastrointestinal Videoscope Recalled by Olympus Corporation...

The Issue: Sterilization failures when devices are sterilized per the Reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Carestream Health, Inc.

Recalled Item: The DRX-Revolution Mobile X-Ray System is a diagnostic mobile x-ray Recalled...

The Issue: There is a potential for unexpected failure of the electrical components...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Coapt LLC

Recalled Item: Coapt Dome Electrode Recalled by Coapt LLC Due to Patient may experience...

The Issue: Patient may experience minor burn or blistering if device is exposed to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Coapt LLC

Recalled Item: Coapt ControlSeal Electrode Recalled by Coapt LLC Due to Patient may...

The Issue: Patient may experience minor burn or blistering if device is exposed to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Sentinel CH SpA

Recalled Item: IRON assay Recalled by Sentinel CH SpA Due to A high recovery of Iron assay...

The Issue: A high recovery of Iron assay has been observed at some customer sites....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Sentinel CH SpA

Recalled Item: Alinity c Iron Reagent Recalled by Sentinel CH SpA Due to A high recovery of...

The Issue: A high recovery of Iron assay has been observed at some customer sites....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing