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 4938149400 of 52,000 recalls

Medical DeviceDecember 5, 2012· B Braun Medical, Inc.

Recalled Item: Outlook ES pump is intended for use with B. Braun Recalled by B Braun...

The Issue: B. Braun Medical Inc. is informing our customers of a field correction...

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

Class II — Potential Health HazardOngoing
DrugDecember 5, 2012· West-ward Pharmaceutical Corp.

Recalled Item: PredniSONE Tablets Recalled by West-ward Pharmaceutical Corp. Due to...

The Issue: Presence of Foreign Substance: Tablets are being recalled due to gray...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 5, 2012· West-ward Pharmaceutical Corp.

Recalled Item: PredniSONE Tablets Recalled by West-ward Pharmaceutical Corp. Due to...

The Issue: Presence of Foreign Substance: A complaint was received for black specks...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 5, 2012· Teva Pharmaceuticals USA, Inc.

Recalled Item: Copaxone (glatiramer acetate injection) Recalled by Teva Pharmaceuticals...

The Issue: Presence of Foreign Substance: Product is being recalled due to receiving an...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2012· Abbott Laboratories

Recalled Item: Synthroid (Levothyroxine Sodium) tablets Recalled by Abbott Laboratories Due...

The Issue: Labeling: Error on Declared Strength. Product labeled to contain 150 mcg...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2012· Amedra Pharmaceuticals LLC

Recalled Item: Dextroamphetamine Sulfate Extended Release Capsules Recalled by Amedra...

The Issue: Failed Dissolution Specifications: The affected lots may not meet the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2012· Amedra Pharmaceuticals LLC

Recalled Item: Dextroamphetamine Sulfate Extended Release Capsules Recalled by Amedra...

The Issue: Failed Dissolution Specifications: The affected lots may not meet the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2012· Johnson & Johnson

Recalled Item: Clean & Clear advantage Recalled by Johnson & Johnson Due to Superpotent...

The Issue: Superpotent (Single Ingredient Drug): salicylic acid

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

Class III — Low RiskOngoing
Refund
DrugDecember 4, 2012· Green Valley Drugs

Recalled Item: Cyanocobalamin 1000 mcg/ml Recalled by Green Valley Drugs Due to...

The Issue: Non-Sterility: Green Valley Drugs received positive sterility results from...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 4, 2012· Amedra Pharmaceuticals LLC

Recalled Item: Dextroamphetamine Sulfate Extended Release Capsules Recalled by Amedra...

The Issue: Failed Dissolution Specifications: The affected lots may not meet the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2012· Green Valley Drugs

Recalled Item: Methylprednisolone Preservative Free 40 mg/ml Injectible Suspension Recalled...

The Issue: Non-Sterility: Green Valley Drugs received positive sterility results from...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 4, 2012· Abbott Molecular

Recalled Item: Abbott m2000sp Instrument Recalled by Abbott Molecular Due to An issue with...

The Issue: An issue with the m2000sp Instrument software has been identified whereby,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS F 8 CALC 13.5MM LG Packaging: Product is Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS 8IN CALC 1.5/19.5 Packaging: Product is packed within Recalled by...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS L 9IN CALC 2.25/19.5 Packaging: Product is packed Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS R 9IN CALC 2.25/16.5 Packaging: Product is packed Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS L 9IN CALC 2.25/15.0 Packaging: Product is packed Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS 8IN CALC 1.5/18.0 Packaging: Product is packed within Recalled by...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· Medtronic Neuromodulation

Recalled Item: Medtronic Recalled by Medtronic Neuromodulation Due to Medtronic has...

The Issue: Medtronic has identified 140 Restore DBS Extension Kits (model numbers 7482,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS R 9IN CALC 2.25/18 Packaging: Product is packed Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing