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. 2,645 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,645 in last 12 months

Showing 1312113140 of 13,463 recalls

DrugJuly 25, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.075 mg. Recalled by Lloyd Inc. of Iowa Due to Subpotent; 9-month...

The Issue: Subpotent; 9-month stability interval

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.050 mg. Recalled by Lloyd Inc. of Iowa Due to Subpotent; 9-month...

The Issue: Subpotent; 9-month stability interval

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2012· American Health Packaging

Recalled Item: Topiramate Tablets Recalled by American Health Packaging Due to Labeling:...

The Issue: Labeling: Label Mix-Up: A typographical error in the product form on the...

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

Class III — Low RiskOngoing
Refund
DrugJuly 24, 2012· Cadence Pharmaceuticals

Recalled Item: OFIRMEV (acetaminophen) injection Recalled by Cadence Pharmaceuticals Due to...

The Issue: Presence of Particulate Matter: The firm initiated the recall due to visible...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2012· Stat Rx USA

Recalled Item: Tizanidine (Generic for: Zanaflex) Recalled by Stat Rx USA Due to Labeling:...

The Issue: Labeling: Label Mix-Up; Some bottles of Tizanidine 4mg Tablets, had the...

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

Class III — Low RiskOngoing
Refund
DrugJuly 23, 2012· American Health Packaging

Recalled Item: Mercaptopurine Tablets Recalled by American Health Packaging Due to Failed...

The Issue: Failed USP Dissolution Test Requirements: This sub-recall is in response to...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 19, 2012· Abbott Laboratories

Recalled Item: Synthroid (levothyroxine sodium) Tablets USP Recalled by Abbott Laboratories...

The Issue: Defective Container: A number of Synthroid bottles have a localized thin...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 19, 2012· Abbott Laboratories

Recalled Item: Synthroid (levothyroxine sodium) Tablets USP Recalled by Abbott Laboratories...

The Issue: Defective Container: A number of Synthroid bottles have a localized thin...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 19, 2012· Abbott Laboratories

Recalled Item: Synthroid (levothyroxine sodium) Tablets USP Recalled by Abbott Laboratories...

The Issue: Defective Container: A number of Synthroid bottles have a localized thin...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2012· Fougera Pharmaceuticals Inc.

Recalled Item: Fougera Ketoconazole Cream 2% Recalled by Fougera Pharmaceuticals Inc. Due...

The Issue: Failed Impurities/Degradation Specifications: Ketoconazole Cream 2% is the...

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

Class III — Low RiskOngoing
Refund
DrugJuly 18, 2012· LNK International, Inc.

Recalled Item: Walgreens ASPIRIN FREE TENSION HEADACHE Recalled by LNK International, Inc....

The Issue: Incorrect/Undeclared Excipients: The firm recalled specific lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 16, 2012· Coral Rock Man, Inc.

Recalled Item: X-ROCK 3 Day Pill For Men Recalled by Coral Rock Man, Inc. Due to Marketed...

The Issue: Marketed Without an Approved NDA/ANDA: Products tested positive for...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 16, 2012· Coral Rock Man, Inc.

Recalled Item: Z-ROCK All Natural Male Supplement. 1 capsule blister pack Recalled by Coral...

The Issue: Marketed Without an Approved NDA/ANDA: Products tested positive for...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 12, 2012· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...

The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2012· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...

The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2012· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...

The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2012· Actavis

Recalled Item: Fentanyl Transdermal System Recalled by Actavis Due to Subpotent; some...

The Issue: Subpotent; some patches may not contain fentanyl gel

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...

The Issue: cGMP Deviations; does not meet in process specification requirements

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...

The Issue: cGMP Deviations; does not meet in process specification requirements

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...

The Issue: cGMP Deviations; does not meet in process specification requirements

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

Class II — Potential Health HazardOngoing
Refund