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.
Showing 12881–12900 of 13,463 recalls
Recalled Item: SEPP 70% Isopropanol (isopropyl alcohol) 70% v/v Recalled by CareFusion 213,...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Donor Prep Kit containing 1 FREPP (70% isopropyl alcohol) Recalled by...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEPP 10% Povidone Iodine Solution USP (1% available Iodine Recalled by...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blood Culture Prep Kit II containing 1 FREPP (70% isopropyl alcohol)...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEPP 2% Iodine Tincture USP (47% v/v Ethyl Alcohol Recalled by CareFusion...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Voltaren 1% Gel Recalled by Physicians Total Care, Inc. Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Expiration Date; This recall is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Labeling Wrong Barcode; It may display wrong product code 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibric Acid Recalled by Mutual Pharmaceutical Company, Inc. Due to...
The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibric Acid Recalled by Mutual Pharmaceutical Company, Inc. Due to...
The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FIBRICOR (fenofibric acid) Tablets Recalled by Mutual Pharmaceutical...
The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QUELICIN (succinylcholine chloride) Injection Recalled by Hospira Inc. Due...
The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Acetate Injection Recalled by Hospira Inc. Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diazepam Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefdinir for Oral Suspension Recalled by Teva Pharmaceuticals USA, Inc. Due...
The Issue: Defective Container: This recall is being carried out due to the potential...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Furosemide Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...
The Issue: Tablets/Capsules Imprinted With Wrong ID: Pharmaceuticals are imprinted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Visible particulate embedded in vials was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ethambutol Hydrochloride Tablets USP Recalled by Lupin Pharmaceuticals Inc....
The Issue: Failed Impurities/Degradation Specifications: This product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novartis Lamisil AT Cream for Jock Itch (terbinafine hydrochloride 1%...
The Issue: Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lamisil AT Cream (terbinafine hydrochloride 1% antifungal) Recalled by...
The Issue: Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.