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. 2,489 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,489 in last 12 months

Showing 2104121060 of 28,172 recalls

Medical DeviceNovember 20, 2015· Steris Corporation

Recalled Item: AMSCO¿ Warming Cabinet. Manufactured by: STERIS Corporation To raise the...

The Issue: The firm discovered that information printed on the quick magnet is...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2015· Bigwall Enterprises

Recalled Item: WARM STEAM Personal Steam Inhaler-Adjustable control to regulate flow of...

The Issue: "The public reason for the recall is that the product is being recalled out...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2015· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific is voluntarily recalling its Chariot" Guiding Sheath. To...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 19, 2015· Biomerieux

Recalled Item: Etest¿ PIP/TAZO/CON-4 PTC 256 - Foam of 100 tests WW. Recalled by Biomerieux...

The Issue: Due to the potential for reporting erroneous results for...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 19, 2015· Biomerieux

Recalled Item: Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW...

The Issue: Due to the potential for reporting erroneous results for...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 19, 2015· Biomerieux

Recalled Item: Etest¿ PIP/TAZO/CON-4 PTC 256 - Foam of 100 tests US. Recalled by Biomerieux...

The Issue: Due to the potential for reporting erroneous results for...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 19, 2015· Biomerieux

Recalled Item: Etest¿ PIP/TAZO/CON-4 PTC 256 -pack of 30 tests US. Etest¿ Recalled by...

The Issue: Due to the potential for reporting erroneous results for...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 18, 2015· Radiometer America Inc

Recalled Item: TCM CombiM Modules 903-111 Recalled by Radiometer America Inc Due to...

The Issue: Radiometer America, Inc. is recalling TCM CombiM on rare occasions they may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2015· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 Radiation therapy system Recalled by Mevion Medical Systems,...

The Issue: The treatment table positioning belt can slip gear positions, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2015· Rainbow Specialty & Health Products

Recalled Item: Dressol-X Recalled by Rainbow Specialty & Health Products Due to Rainbow...

The Issue: Rainbow Specialty & Health Products initiated a field action for Dressol-X...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2015· Rainbow Specialty & Health Products

Recalled Item: Dressit-X Recalled by Rainbow Specialty & Health Products Due to Rainbow...

The Issue: Rainbow Specialty & Health Products initiated a field action for Dressol-X...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Software version VD10E for Syngo X-Workplace Recalled by Siemens Medical...

The Issue: Potential post-processing software issue when using tabcard "4D" on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer K2 EDTA (K2E) 5.4mg Plus Blood Collection Tubes. Recalled by...

The Issue: Some tubes were manufactured with the stopper not fully inserted into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Owens & Minor Distribution, Inc.

Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....

The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Owens & Minor Distribution, Inc.

Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....

The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Olympus Corporation of the Americas

Recalled Item: Olympus ENDOEYE HD II Video Telescopes. Models WA50040A ENDOEYE HD II...

The Issue: A damaged temperature sensor at the ENDOEYE tip caused the distal end to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Owens & Minor Distribution, Inc.

Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....

The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Biomet, Inc.

Recalled Item: Biomet Integral Centralizer Hip System Recalled by Biomet, Inc. Due to PMMA...

The Issue: PMMA is listed as a material on the label but the product does not contain PMMA.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: ProScreen 10 Panel Cup Recalled by Ameditech Inc Due to Ameditechs Drugs of...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

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

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: ProScreen 10 Panel Dip Card Recalled by Ameditech Inc Due to Ameditechs...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

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

Class III — Low RiskOngoing