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 2638126400 of 28,172 recalls

Medical DeviceFebruary 14, 2013· Zimmer, Inc.

Recalled Item: Zimmer Patient Helper Bed Frame Adapter Assembly The bed frame Recalled by...

The Issue: The bed frame adapter assemblies may have a weak weld where the patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Steris Corporation

Recalled Item: AMSCO C and AMSCO 400 Steam Sterilizers designed for sterilization Recalled...

The Issue: The control boards alarm set points and temperature tolerances allowed for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Oculus Innovative Sciences Inc

Recalled Item: Atrapro Antipruritic Hydrogel Recalled by Oculus Innovative Sciences Inc Due...

The Issue: Out of specification result - stability test failure of free available...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Intellispace Portal (ISP) Philips Medical Systems (Cleveland) Recalled by...

The Issue: Philips was notified of a problem using the IntelliSpace Portal with...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Integra LifeSciences Corp.

Recalled Item: Integra(R) Jarit(R) Monopolar Cable (Catalogue No. 600-290). For use in...

The Issue: Addendum to the Instructions for Use. The addendum emphasizes the warnings...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Beckman Coulter Inc.

Recalled Item: Synchron LXi 725 Clinical System Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter is initiating a recall due to a defective newly released...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Beckman Coulter Inc.

Recalled Item: Access Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is initiating a recall due to a defective newly released...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Beckman Coulter Inc.

Recalled Item: UniCel DxC 600i Synchron Access Clinical System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is initiating a recall due to a defective newly released...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Polymedco, Inc

Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...

The Issue: The test strips in the affected product lots of the OC Light immunological...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Beckman Coulter Inc.

Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is initiating a recall due to a defective newly released...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Polymedco, Inc

Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...

The Issue: The test strips in the affected product lots of the OC Light immunological...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2013· Innominata Dba Genbio

Recalled Item: ANTI-BORRELIA (LYME) MICROPLATE EIA Kit Recalled by Innominata Dba Genbio...

The Issue: Multiple incidents of low-reacting assay plates.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2013· Elekta, Inc.

Recalled Item: Monaco RTP System. Radiation treatment planning. Recalled by Elekta, Inc....

The Issue: The beam is displayed at the "gantry" angle, but the dose is calculated at...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2013· Microbiologics Inc

Recalled Item: Microbiologics KWIK-QC SLIDES ( KWIK-QC Acid Fast Stain Slides and Recalled...

The Issue: Microbiologics Inc is initiating a voluntary recall on products KWIK-QC Acid...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2013· Zimmer, Inc.

Recalled Item: Zimmer NexPosure Recalled by Zimmer, Inc. Due to Possibility that the inner...

The Issue: Possibility that the inner pouch may be compromised. The product is packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2013· Ultradent Products, Inc.

Recalled Item: Avex CX Suite Recalled by Ultradent Products, Inc. Due to Orthodontic...

The Issue: Orthodontic brackets distributed was incorrectly labeled.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 8, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare LOGIQ S8 (with software revisions R1.1.1 and R1.5.1) Recalled...

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

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic DBS Lead Kit for Deep Brain Stimulation Recalled by Medtronic...

The Issue: There is a potential for lead damage due to the use of the lead cap provided...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 8, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic DBS Therapy for Dystonia Kit Recalled by Medtronic Neuromodulation...

The Issue: There is a potential for lead damage due to the use of the lead cap provided...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 7, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Ortho-Clinical...

The Issue: Ortho-Clinical Diagnostics, Inc. (OCD) determined that extension springs on...

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

Class II — Potential Health HazardOngoing