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. 905 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
905 in last 12 months

Showing 49961–49980 of 52,000 recalls

Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Battery Recalled by Terumo Cardiovascular Systems Corporation Due to Terumo...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Alphatec Spine, Inc.

Recalled Item: ILLlCO¿ MIS Posterior Fixation System Recalled by Alphatec Spine, Inc. Due...

The Issue: The firm initiated the recall because the stainless steel guide-wire of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Stryker Communications, Inc.

Recalled Item: (l) Visum Halogen Surgical Light Recalled by Stryker Communications, Inc....

The Issue: Stryker has become aware that there is a low likelihood of incomplete...

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

Class II — Potential Health HazardOngoing
FoodSeptember 25, 2012· Chattanooga Bakery Inc

Recalled Item: Moon Pie(R) Crunch Peanut Butter Recalled by Chattanooga Bakery Inc Due to...

The Issue: Peanut Butter Crunch Moon Pies were manufactured with peanut butter supplied...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 24, 2012· Richmond Baking of Georgia Inc

Recalled Item: MJM Tropical Treats Recalled by Richmond Baking of Georgia Inc Due to...

The Issue: Product contains undeclared allergen: Soy Lecithin.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 24, 2012· Winco Mfg., LLC

Recalled Item: Cozy Comfort Premier Recliner 5580 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...

The Issue: The performance of the chemicals in the foam and vinyl are not consistent...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2012· Winco Mfg., LLC

Recalled Item: PREMIER LIFECARE RECLINER 5400 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...

The Issue: The performance of the chemicals in the foam and vinyl are not consistent...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2012· Winco Mfg., LLC

Recalled Item: PREMIER CARE RECLINER 5570/5574 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...

The Issue: The performance of the chemicals in the foam and vinyl are not consistent...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2012· Winco Mfg., LLC

Recalled Item: Designer Care Cliner 6700/6704/6710 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...

The Issue: The performance of the chemicals in the foam and vinyl are not consistent...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Centrifugal System Control module Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received one report of loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2012· Mindray DS USA, Inc. d.b.a. Mindray North America

Recalled Item: Mindray V12 Size: 320 mm X 320 mm X 450 Recalled by Mindray DS USA, Inc....

The Issue: Mindray has identified an issue with the V Series Monitor where the monitors...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Centrifugal System Control module System 9000 The Sarns Centrifugal...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received one report of loss of...

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

Class II — Potential Health HazardOngoing