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. 2,448 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,448 in last 12 months

Showing 2774127760 of 28,172 recalls

Medical DeviceApril 11, 2012· Siemens Medical Solutions USA, Inc.

Recalled Item: E.CAM emission computed tomography system used to detect or image Recalled...

The Issue: Radial motor drives replaced during a customer service action were...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2012· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia E is a multi-purpose SPECT system used to detect Recalled by Siemens...

The Issue: Radial motor drives replaced during a customer service action were...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 10, 2012· Linvatec Corp. dba ConMed Linvatec

Recalled Item: "***SENTINEL***Cannulated Drill Bit***S8580***8 X 229mm (9")***CONMED...

The Issue: Linvatec Corporation dba ConMed Linvatec in Largo, FL is recalling the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2012· Kerr Corporation

Recalled Item: The brand name of the device is Laser Loupes Recalled by Kerr Corporation...

The Issue: The firm initiated the recall for Laser Loupes because the ink used to mark...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2012· Linvatec Corp. dba ConMed Linvatec

Recalled Item: "***SENTINEL***Cannulated Drill Bit***S8585***8.5 X 229mm (9")***CONMED...

The Issue: Linvatec Corporation dba ConMed Linvatec in Largo, FL is recalling the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2012· Linvatec Corp. dba ConMed Linvatec

Recalled Item: "***All in one CrossFT***Punch***PFT-00M***4.5mm to 6.5mm***CONMED LINVATEC...

The Issue: ConMed Linvatec is recalling the product due to the punch being...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2012· Gulf Fiberoptics, Inc.

Recalled Item: GMF-RC65 Replacement Surgical Headlight Cable for Cogent Microlink. GMF-RC65...

The Issue: The GMF-RC65 Replacement Surgical Headlight Cable for Cogent Microlink falls...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2012· Invacare Corporation

Recalled Item: TDX SP Power Wheelchair Recalled by Invacare Corporation Due to Invacare...

The Issue: Invacare Corporation decided to recall the product because of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2012· Etac Supply Center Ab

Recalled Item: Etac¿ Ono Walker Recalled by Etac Supply Center Ab Due to The recall has...

The Issue: The recall has been initiated because there is the potential that users may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2012· Steris Corporation

Recalled Item: STERIS 5085 and 5085 SRT Surgical Tables Recalled by Steris Corporation Due...

The Issue: STERIS has learned from Customer feedback and field service experience that...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima Mobile X-ray System. The GE Automatic Mobile Recalled...

The Issue: GE Healthcare has become aware of a software issue on the interface of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2012· Ethicon, Inc.

Recalled Item: Ethicon Surgiflo Hemostatic Matrix Kit with Thrombin Plus Flex Tip Recalled...

The Issue: The lyophilized thrombin component of the Surgiflo Hemostatic Matrix kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2012· Beckman Coulter Inc.

Recalled Item: Unicel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is recalling the UniCel DxH 800 Coulter Cellular Analysis...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Restoration Modular Cone Body Trials Stryker Ireland...

The Issue: Stryker Orthopaedics has become aware of a burr, or a metal shaving,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2012· Hill-Rom, Inc.

Recalled Item: Affinity Four Birthing Bed P3700 Product Usage: The Affinity Recalled by...

The Issue: During review of our last braking system via that field corrective action,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2012· Medical Components, Inc dba MedComp

Recalled Item: MRCTT80041 MedComp 8F Plastic Pro-Fuse(R) CT Low Profile Port with Recalled...

The Issue: Product was packaged with the incorrect port and does not match the label....

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2012· Greiner Bio-One North America, Inc.

Recalled Item: Vacuette Quickshield Complete Plus Recalled by Greiner Bio-One North...

The Issue: : The Quickshield Complete Plus may have a defect (split at the base), which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2012· Impact Instrumentation, Inc.

Recalled Item: Model 324JL On-Board Suction System Intended use: On-board suction system...

The Issue: A shipment mix-up took place.

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

Class III — Low RiskOngoing
Medical DeviceMarch 29, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius NaturaLyte Liquid Acid Concentrate Product Codes: 08-0231-4...

The Issue: Risk of Alkalosis with acetate containing dialysis acid concentrates

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

Class I — Serious Health HazardOngoing