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 1306113080 of 13,463 recalls

DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Methylprednisolone Acetate 80 mg/mL Injection Recalled by New England...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Dexamethasone Sodium Phosphate 4 mg/mL vials PF Recalled by New England...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Hyaluronidase 150 u/ml PF Recalled by New England Compounding Center Due to...

The Issue: Lack of Assurance of Sterility

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: 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
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: 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· 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: 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 20, 2012· Globe All Wellness, LLC

Recalled Item: SLIM XTREME Herbal Slimming Capsule Recalled by Globe All Wellness, LLC Due...

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

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 20, 2012· Genentech Inc

Recalled Item: Nutropin AQ NuSpin 20 (somatropin (rDNA origin) injection} 20 mg/ 2mL...

The Issue: Miscalibrated and/or Defective Delivery System: Genentech has received...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2012· Genentech Inc

Recalled Item: Nutropin AQ NuSpin 10 (somatropin (rDNA origin) injection} 10 mg/ 2mL...

The Issue: Miscalibrated and/or Defective Delivery System: Genentech has received...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2012· Sandoz Incorporated

Recalled Item: Children's Cetirizine HCl Chewable Tablets 5 mg Recalled by Sandoz...

The Issue: Impurity/Degradation; exceeded impurity specification at the 8 and 15 month...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 17, 2012· DermaCare, Inc.

Recalled Item: UP & UP brand Recalled by DermaCare, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non-Sterile Products: Laboratory findings of high...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2012· DermaCare, Inc.

Recalled Item: UP & UP brand Recalled by DermaCare, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non-Sterile Products: Laboratory findings of high...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2012· Sandoz Incorporated

Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by Sandoz Incorporated Due to...

The Issue: Impurities/Degradation Products: An out of specification result for a known...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 12, 2012· Sandoz Incorporated

Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by Sandoz Incorporated Due to...

The Issue: Impurities/Degradation Products: An out of specification result for a known...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 10, 2012· Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Recalled Item: HYDROCODONE BITARTRATE and ACETAMINOPHEN TABLETS Recalled by Vintage...

The Issue: Superpotent (Multiple Ingredient) Drug: Confirmed customer complaints of...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 6, 2012· Church & Dwight Inc

Recalled Item: Orajel Kids My Way! Anticavity Fluoride (sodium fluoride) toothpaste...

The Issue: CGMP Deviations: Product was made with an incorrect ingredient, Laureth-9...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: DRxChoice Fiber Capsules Recalled by Raritan Pharmaceuticals, Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund