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. 1,734 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
1,734 in last 12 months

Showing 4654146560 of 49,744 recalls

Medical DeviceMarch 26, 2013· Cardinal Health, Medical Products & Services

Recalled Item: Presource PBDS Recalled by Cardinal Health, Medical Products & Services Due...

The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Crimpers Recalled by Edwards Lifesciences, LLC Due to...

The Issue: Holes in the sterile barrier pouch may be caused by handling of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2013· Cardinal Health, Medical Products & Services

Recalled Item: Presource PBDS Recalled by Cardinal Health, Medical Products & Services Due...

The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2013· Cardinal Health, Medical Products & Services

Recalled Item: Presource PBDS Recalled by Cardinal Health, Medical Products & Services Due...

The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2013· Cardinal Health, Medical Products & Services

Recalled Item: Presource PBDS Recalled by Cardinal Health, Medical Products & Services Due...

The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2013· Cardinal Health, Medical Products & Services

Recalled Item: Presource PBDS Recalled by Cardinal Health, Medical Products & Services Due...

The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2013· Cardinal Health, Medical Products & Services

Recalled Item: A) Presource PBDS Recalled by Cardinal Health, Medical Products & Services...

The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2013· GE Healthcare, LLC

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

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

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2013· GE Healthcare, LLC

Recalled Item: GE PET Discovery 610 Recalled by GE Healthcare, LLC Due to GE Healthcare has...

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

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Triathlon Femoral Distal Augment- Left Recalled by...

The Issue: Stryker Orthopaedics received a report that a label on the external...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2013· Microbiologics Inc

Recalled Item: KWIK-STIK(TM) Recalled by Microbiologics Inc Due to Some of the KWIK-STIK...

The Issue: Some of the KWIK-STIK Catalog #01023P Campylobacter coli, Lot# 1023-05-7,...

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

Class III — Low RiskOngoing
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Dexamethasone PF Recalled by Pallimed Solutions Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: DMSO Aqueous Irrigation 50% Recalled by Pallimed Solutions Due to Lack of...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Vancomycin Ophthalmic PF Recalled by Pallimed Solutions Due to Lack of...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: MIC with B6 and B12 Recalled by Pallimed Solutions Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Atropine Injection Recalled by Pallimed Solutions Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Diazepam Injectable Recalled by Pallimed Solutions Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Testosterone Cypionate Injection Recalled by Pallimed Solutions Due to Lack...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Trimix Injection Recalled by Pallimed Solutions Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Cyclosporine Ophthalmic Recalled by Pallimed Solutions Due to Lack of...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund