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. 2,465 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,465 in last 12 months

Showing 2482124840 of 28,172 recalls

Medical DeviceNovember 20, 2013· Boston Scientific Corporation

Recalled Item: TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 10 configuration)...

The Issue: Sterility of device may be compromised due to lack of pouch seal integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2013· Boston Scientific Corporation

Recalled Item: TWISTER PLUS 26mm Rotatable Retrieval Device (Box of 1 configuration)...

The Issue: Sterility of device may be compromised due to lack of pouch seal integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2013· CooperVision Inc.

Recalled Item: Pro clear(R) 1 day Sphere (o mafilcon A) Recalled by CooperVision Inc. Due...

The Issue: Lots were labeled with incorrect expiration dates on secondary package...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2013· CooperVision Inc.

Recalled Item: ClearSight(TM) Toric 1 day (ocufilcon D) Recalled by CooperVision Inc. Due...

The Issue: Lots were labeled with incorrect expiration dates on secondary package...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2013· Sorin Group Italia S.r.l.

Recalled Item: ORCHESTRA/ORCHESTRA PLUS Programmer Recalled by Sorin Group Italia S.r.l....

The Issue: Sorin has voluntarily issued a notification to physicians related to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2013· Boston Scientific Corporation

Recalled Item: TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 5 configuration)...

The Issue: Sterility of device may be compromised due to lack of pouch seal integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2013· Boston Scientific Corporation

Recalled Item: TWISTER PLUS 26mm Rotatable Retrieval Device (Box of 10 configuration)...

The Issue: Sterility of device may be compromised due to lack of pouch seal integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Asante Solutions, Inc.

Recalled Item: Asante Comfort Infusion Set with 110cm tubing & 17mm cannula Recalled by...

The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Ultradent Products, Inc.

Recalled Item: Opal Orthodontics by Ultradent. Avex CX2 Ceramic Orthodontic Brackets Avex...

The Issue: Ultradent Products Inc. is recalling various lots of Avex CX2 Orthodontic...

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

Class III — Low RiskOngoing
Medical DeviceNovember 19, 2013· Atrium Medical Corporation

Recalled Item: Atrium Oasis Dry Suction Water Seal ATS (Autotransfusion) Blood Recovery...

The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Atrium Medical Corporation

Recalled Item: Atrium Ocean Water Seal Chest Drain ATS (Autotransfusion) Blood Recovery...

The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Atrium Medical Corporation

Recalled Item: Atrium Oasis Dry Suction Water Seal ATS (Autotransfusion) Blood Recovery...

The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Atrium Medical Corporation

Recalled Item: Atrium Express Dry Seal ATS (Autotransfusion) Blood Recovery System Chest...

The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Atrium Medical Corporation

Recalled Item: Atrium Ocean Water Seal Chest Drain ATS (Autotransfusion) Blood Recovery...

The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Atrium Medical Corporation

Recalled Item: Atrium Express Dry Seal ATS (Autotransfusion) Blood Recovery System Chest...

The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Porous Patella Drill Guide-26mm dia./10mm...

The Issue: This is an expansion of the June 2013 recall of NexGen Micro components....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Asante Solutions, Inc.

Recalled Item: Asante Conset Infusion Set with 60cm tubing & 9mm cannula packaged in...

The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Asante Solutions, Inc.

Recalled Item: Asante Comfort Infusion Set with 110cm tubing & 13mm cannula packaged in...

The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution CR Articular Surface Provisional-Yellow 9mm...

The Issue: This is an expansion of the June 2013 recall of NexGen Micro components....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Porous Patella Drill Guide-29mm dia./10mm...

The Issue: This is an expansion of the June 2013 recall of NexGen Micro components....

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

Class II — Potential Health HazardOngoing