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. 2,502 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,502 in last 12 months

Showing 2086120880 of 28,172 recalls

Medical DeviceDecember 4, 2015· Steris Corporation

Recalled Item: Quick Connects. Steris Corporation. Model numbers: QKC1736E Recalled by...

The Issue: The firm discovered that one of the hysteroscope models listed for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Del Medical, Inc.

Recalled Item: VS300 radiographic Cassette Holder or Wall Stand. For use in Recalled by Del...

The Issue: The wall stand cassette holder can suddenly fall to the bottom of its...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Ethicon, Inc.

Recalled Item: Gynecare Thermachoice III Uterine Balloon Therapy System Ethicon Recalled by...

The Issue: Stability data does not substantiate the labeled two-year shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...

The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...

The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...

The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...

The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Del Medical, Inc.

Recalled Item: VS200 radiographic Cassette Holder or Wall Stand. For use in Recalled by Del...

The Issue: The wall stand cassette holder can suddenly fall to the bottom of its...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...

The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker Position Pro Mattress. Mattress Recalled by Stryker Medical Division...

The Issue: Potential for power cord to melt; hazards include electric shock and fire.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Teleflex Medical

Recalled Item: Servo Humidifier 163 Recalled by Teleflex Medical Due to Cracks may occur at...

The Issue: Cracks may occur at the 15mm and 22mm ISO female connector.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Smiths Medical ASD Inc.

Recalled Item: Medfusion Model 3500 and 4000 Syringe Infusion Pumps and Medfusion Recalled...

The Issue: There have been intermittent issues with Supercap POST (power on self-test)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Best Practice Kits containing certain production lots of Endo GIA Recalled...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Covidien Endo GIA Ultra Universal Standard Stapler Handle Recalled by...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Covidien Endo GIA Ultra Universal 12 mm Short Stapler Handle Recalled by...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Covidien Endo GIA Ultra Universal 12 mm XL Stapler Handle Recalled by...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Gsi Group Inc

Recalled Item: PRN 50-M+ Recalled by Gsi Group Inc Due to The item was recalled due to an...

The Issue: The item was recalled due to an increased user/patient risk of exposure to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Partners In Medicine Llc

Recalled Item: CNSystems TASK FORCE MONITOR 3040i Recalled by Partners In Medicine Llc Due...

The Issue: Device non-conformity which may lead to an incorrect oscillometric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· JosNoe Medical, Inc.

Recalled Item: PS-500 Scope Warmer Recalled by JosNoe Medical, Inc. Due to Damage to...

The Issue: Damage to package seals potentially compromising sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· 3M Company - Health Care Business

Recalled Item: 3M Coban Self-Adherent Wrap Shipper carton label identified the product...

The Issue: Product mislabeled as latex free. Actual Catalog number 1581, lot 2020-10AN....

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

Class II — Potential Health HazardOngoing