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

52,000 total recalls
916 in last 12 months

Showing 49981–50000 of 52,000 recalls

Medical DeviceSeptember 24, 2012· Varian Medical Systems, Inc. Oncology Systems

Recalled Item: ARIA Radiation Oncology Recalled by Varian Medical Systems, Inc. Oncology...

The Issue: An anomaly has been identified with the ARIA Oncology Information System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2012· Greatbatch Medical

Recalled Item: Biosense Webster MobiCath Bi-Directional Guiding Sheath. Small Curve catalog...

The Issue: We are notifying you of a potential interaction between therapeutic...

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 21, 2012· Asahi Kasei Medical Co., Ltd., Okatomi Plant

Recalled Item: Asahi KASEI Recalled by Asahi Kasei Medical Co., Ltd., Okatomi Plant Due to...

The Issue: Asahi became aware of a negative trend for rate of the adverse events that...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2012· Asahi Kasei Medical Co., Ltd., Okatomi Plant

Recalled Item: Asahi KASEI Recalled by Asahi Kasei Medical Co., Ltd., Okatomi Plant Due to...

The Issue: Asahi became aware of a negative trend for rate of the adverse events that...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2012· Asahi Kasei Medical Co., Ltd., Okatomi Plant

Recalled Item: Asahi KASEI Recalled by Asahi Kasei Medical Co., Ltd., Okatomi Plant Due to...

The Issue: Asahi became aware of a negative trend for rate of the adverse events that...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2012· Asahi Kasei Medical Co., Ltd., Okatomi Plant

Recalled Item: Asahi KASEI Recalled by Asahi Kasei Medical Co., Ltd., Okatomi Plant Due to...

The Issue: Asahi became aware of a negative trend for rate of the adverse events that...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2012· Asahi Kasei Medical Co., Ltd., Okatomi Plant

Recalled Item: Asahi KASEI Recalled by Asahi Kasei Medical Co., Ltd., Okatomi Plant Due to...

The Issue: Asahi became aware of a negative trend for rate of the adverse events that...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2012· Asahi Kasei Medical Co., Ltd., Okatomi Plant

Recalled Item: Asahi KASEI Recalled by Asahi Kasei Medical Co., Ltd., Okatomi Plant Due to...

The Issue: Asahi became aware of a negative trend for rate of the adverse events that...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2012· Asahi Kasei Medical Co., Ltd., Okatomi Plant

Recalled Item: Asahi KASEI Recalled by Asahi Kasei Medical Co., Ltd., Okatomi Plant Due to...

The Issue: Asahi became aware of a negative trend for rate of the adverse events that...

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

Class II — Potential Health HazardOngoing
DrugSeptember 21, 2012· Baxter Healthcare Corp.

Recalled Item: 5% Dextrose Injection USP Recalled by Baxter Healthcare Corp. Due to...

The Issue: Chemical Contamination: The IV solutions were packaged in AVIVA containers...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2012· Watson Laboratories Inc

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets USP Recalled by Watson...

The Issue: Superpotent (Multiple Ingredient) Drug: There is the potential for oversized...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 21, 2012· Baxter Healthcare Corp.

Recalled Item: 10% Dextrose Injection USP Recalled by Baxter Healthcare Corp. Due to...

The Issue: Chemical Contamination: The IV solutions were packaged in AVIVA containers...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2012· Baxter Healthcare Corp.

Recalled Item: Lactated Ringer's Injection USP Recalled by Baxter Healthcare Corp. Due to...

The Issue: Chemical Contamination: The IV solutions were packaged in AVIVA containers...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2012· Baxter Healthcare Corp.

Recalled Item: 5% Dextrose and 0.45% Sodium Chloride Injection USP Recalled by Baxter...

The Issue: Chemical Contamination: The IV solutions were packaged in AVIVA containers...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2012· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp. Due...

The Issue: Chemical Contamination: The IV solutions were packaged in AVIVA containers...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Fortified Vanilla Dietary Supplement Packaged under the labels Stronger...

The Issue: Protein supplement fails to declare allergen: milk

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Recovery Vanilla (also labeled Post Workout) Recalled by Maine Natural...

The Issue: Protein supplement fails to declare allergens: milk, shellfish

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Endurance Daily Chocolate Dietary Supplement Packaged under the label:...

The Issue: Protein supplement fails to declare allergens milk

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Endurance Pre Race Pina Colada Recalled by Maine Natural Health, Inc. Due to...

The Issue: Protein supplement fails to declare allergens: milk

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

Class I — Serious Health HazardOngoing
Refund