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. 1,036 recalls have been distributed to Tennessee in the last 12 months.
Showing 18941–18960 of 52,000 recalls
Recalled Item: BodyGuard Microset w/ 0.2 mic filter and lower y-site with female luer...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard set with Female Luer Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Childrens Dimetapp Cold & Cough Recalled by Glaxosmithkline Consumer...
The Issue: Defective Delivery System: the dosing cups are missing graduations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Childrens Robitussin Honey Cough and Chest Congestion DM Recalled by...
The Issue: Defective Delivery System: the dosing cups are missing graduations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Verigene Processor SP with assay Luminex Recalled by Luminex Corporation Due...
The Issue: An instrument failure mode that may result in a Blood Culture Gram Positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERWAND XL 4Fr 8cm Maximum Barrier Kit (Introducer with an Recalled by...
The Issue: Convenience kit mislabeled with the incorrect catheter effective length on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Processor SP with assay: Luminex Recalled by Luminex Corporation...
The Issue: An instrument failure mode that may result in a Blood Culture Gram Positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tropical Lip Moisturizer Recalled by Yusef Manufacturing Laboratories, LLC...
The Issue: Superpotent Drug: The beginning portion of the batch appears to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl
The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl
The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clozapine Tablets USP tablet Recalled by Aurobindo Pharma USA Inc. Due to...
The Issue: Presence of foreign tablet: Consumer complaint of Clozapine Tablets 50mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl
The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by The Harvard...
The Issue: CGMP Deviation: Potential presence of Nitrosodimethylamine (NDMA) Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Software 1898072 IPC upgrade v 2.7.3.0 - Product Usage: The Recalled by...
The Issue: During internal testing execution of the next generation of Integrated Power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOW Real Food Raw Macadamia Nuts Unsalted 8 oz retail Recalled by NOW Health...
The Issue: The product tested positive for Salmonella enterica.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Irinotecan HCL Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...
The Issue: Defective Container: Customer complaints received of a crimp defect while...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irinotecan HCL Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...
The Issue: Defective Container: Customer complaints received of a crimp defect while...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PORT-A-CATH¿ II POWER P.A.C. Low Profile" system. Recalled by Smiths Medical...
The Issue: Smiths Medical became aware that one (1) lot of PORT-A-CATH¿ II POWER P.A.C....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nuvasive NVM5 EMG Module Recalled by NuVasive Inc Due to The NVM5 EMG Module...
The Issue: The NVM5 EMG Module kit intended for intraoperative neurophysiologic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.