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 74417460 of 28,172 recalls

Medical DeviceOctober 20, 2022· CoreLink LLC

Recalled Item: CoreLink LLC Recalled by CoreLink LLC Due to Specific lots of FLXfit...

The Issue: Specific lots of FLXfit implants have internal components that may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Sensititre Plate Recalled by Remel Inc Due to An internal...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· CooperSurgical, Inc.

Recalled Item: NEO-fit Neonatal Endotracheal Tube Grip Recalled by CooperSurgical, Inc. Due...

The Issue: Firm has received 11 complaints involving a loose or detached metal clips,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2022· Atrium Medical Corporation

Recalled Item: Atrium Ocean Wet Suction Water Seal Chest Drain- Product Code: 2002-000...

The Issue: Warehouse experienced temperature excursions in July and August 2021. It was...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2022· Baxter Healthcare Corporation

Recalled Item: Hill-Rom Progressa Bed System Recalled by Baxter Healthcare Corporation Due...

The Issue: The compression links on impacted Progressa beds, listed in Appendix A, may...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2022· Accelerate Diagnostics Inc

Recalled Item: Accelerate PhenoTest BC kit Recalled by Accelerate Diagnostics Inc Due to...

The Issue: Due improperly formulated and released bulk lot of fluorescence in situ...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2022· Accelerate Diagnostics Inc

Recalled Item: Accelerate PhenoTest BC kit Recalled by Accelerate Diagnostics Inc Due to...

The Issue: Due improperly formulated and released bulk lot of fluorescence in situ...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2022· Visionsense, Ltd.

Recalled Item: VS3 Iridium - Visionsense Infrared (IR) Fluorescence Miniature Microscope...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2022· Visionsense, Ltd.

Recalled Item: VS3 Iridium Visionsense Infrared (IR) Fluorescence Light Integrator (Beam...

The Issue: Broken Optical fiber cable damage can occur through handling or bending and...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2022· Visionsense, Ltd.

Recalled Item: VS3 Iridium Visionsense Infrared (IR) Fluorescence Miniature Microscope...

The Issue: Broken Optical fiber cable damage can occur through handling or bending and...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2022· Insulet Corporation

Recalled Item: 18239: ASM Omnipod Dash PDM Recalled by Insulet Corporation Due to The firm...

The Issue: The firm has become aware of PDM battery issues, including battery swelling,...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 17, 2022· Steris Corporation

Recalled Item: GI4000 Electrosurgical Unit - intended to deliver electrosurgical outputs to...

The Issue: Two electronic diode components (D1 & D4) placed in the reverse orientation...

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

Class II — Potential Health HazardOngoing