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. 2,603 recalls have been distributed to Tennessee in the last 12 months.
Showing 15501–15520 of 52,000 recalls
Recalled Item: Cyclobenzaprine Hydrochloride Tablets Recalled by Teva Pharmaceuticals USA...
The Issue: CGMP Deviations: Out of specification (OOS) test result for Total Aerobic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyclobenzaprine Hydrochloride Tablets Recalled by Teva Pharmaceuticals USA...
The Issue: CGMP Deviations: Out of specification (OOS) test result for Total Aerobic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Ointment USP Recalled by Teligent Pharma, Inc. Due to Failed...
The Issue: Failed Viscosity Specifications: lot does not meet specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Oral Suspension Recalled by PAI Holdings, LLC. dba Pharmaceutical...
The Issue: Lack of CGMP: This recall is being carried out due to potential for carry...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Erythromycin Topical Solution USP Recalled by Teligent Pharma, Inc. Due to...
The Issue: Defective container: possibility for lack of seal integrity.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cimetidine Hydrochloride Oral Solution 300 mg/5 mL Recalled by PAI Holdings,...
The Issue: Lack of CGMP: This recall is being carried out due to potential for carry...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...
The Issue: Presence of Forein Tablets/Capsules; Venlafaxine Tablets, USP 37.5 mg found...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Epoprostenol Sodium for Injection Recalled by Teva Pharmaceuticals USA Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DAUNOrubicin Hydrochloride Injection 20 mg/4mL Recalled by Teva...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ethosuximide Oral Solution USP 250 mg/5 mL Recalled by PAI Holdings, LLC....
The Issue: Lack of CGMP: This recall is being carried out due to potential for carry...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leucovorin Calcium for Injection Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylprednisolone Acetate Injectable Suspension USP Recalled by Teva...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norepinephrine Bitartrate Injection Recalled by Teva Pharmaceuticals USA Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leucovorin Calcium for Injection Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: OASIS MRI System Recalled by Hitachi Healthcare Americas Corporation Due to...
The Issue: There was no label on the pad packaging or notification in the user manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYMOL Medical Elite X Class Rigid Bronchoscope System Recalled by Lymol...
The Issue: Reprocessing instructions were revised November 15, 2020, to new processes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON Oval MRI System Recalled by Hitachi Healthcare Americas Corporation...
The Issue: There was no label on the pad packaging or notification in the user manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HANA/PROFx CLASSIC FEMORAL HOOK RIGHT Recalled by Mizuho OSI Due to One...
The Issue: One batch of "regular" femoral hooks were incorrectly etched with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON MRI System Recalled by Hitachi Healthcare Americas Corporation Due...
The Issue: There was no label on the pad packaging or notification in the user manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity c CRP Vario Cardiac High Sensitivity Calibrator Kit ( by Sentinel CH...
The Issue: Calibrator vials were incorrectly labeled. Use of incorrectly labeled vials...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.