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. 2,452 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,452 in last 12 months

Showing 3830138320 of 52,000 recalls

Medical DeviceAugust 17, 2015· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi Surgical System P4 software Recalled by Intuitive Surgical, Inc....

The Issue: Complaints regarding the Exposed Knife Blade recoverable fault for the Xi...

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

Class II — Potential Health HazardOngoing
FoodAugust 14, 2015· Interpac Technologies

Recalled Item: think Thin Protein & Fiber Oatmeal Recalled by Interpac Technologies Due to...

The Issue: A small number of think Thin Madagascar Vanilla with Almonds & Pecans...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 14, 2015· Toshiba American Medical Systems Inc

Recalled Item: INFX-8000V Bi-Plane X-Ray Interventional System X-ray systems Recalled by...

The Issue: When a fontal DA (Digital Angiography) acquisition was done, scattered x-ray...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...

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

Class II — Potential Health HazardOngoing
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Bactroban Ointment (mupirocin calcium) Recalled by GlaxoSmithKline, LLC. Due...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Bactroban Cream (mupirocin calcium) Recalled by GlaxoSmithKline, LLC. Due to...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Mupirocin Calcium Cream Recalled by GlaxoSmithKline, LLC. Due to Penicillin...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Bactroban (mupirocin calcium) Nasal Ointment Recalled by GlaxoSmithKline,...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 12, 2015· Abbott Electrophysiology

Recalled Item: FIRMap 60mm Catheter Recalled by Abbott Electrophysiology Due to The...

The Issue: The expiration date was incorrectly printed on the pouch/box labels of 19...

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

Class III — Low RiskOngoing
Medical DeviceAugust 11, 2015· Synthes (USA) Products LLC

Recalled Item: Dynamic Locking Screw System (DLS) 3.7mm & Dynamic Locking Screw (DLS) 5.0mm...

The Issue: DLS pin breakage during planned implant removal, after uneventful and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2015· GE Healthcare

Recalled Item: Centricity Universal Viewer Product Usage: The Centricity Universal Viewer...

The Issue: Images from the Centricity PACS-IW with Universal Viewer and Centricity...

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

Class II — Potential Health HazardOngoing