Product Recalls in Tennessee

Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,740 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
1,740 in last 12 months

Showing 4856148580 of 52,000 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· 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 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· 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: 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
FoodMarch 26, 2013· Publix Super Markets, Inc.

Recalled Item: Publix Deli Tri Fruit and Grain Salad with red rice Recalled by Publix Super...

The Issue: Product may be adulterated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMarch 25, 2013· Decoty Coffee Company, Inc

Recalled Item: Taco Seasoning Recalled by Decoty Coffee Company, Inc Due to Undeclared...

The Issue: Recently, DeCoty Taco Seasoning, 1.25 lb (Lot numbers 010111-021313) and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
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: Verapamil 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: 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: Hydroxyprogesterone CAPR.(G.S.) 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: Nandrolone Decanoate Injectable 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