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 18201–18220 of 52,000 recalls
Recalled Item: CLIA Waived Rapid Drug Test (AMT Item Number/ AMT Description): Recalled by...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Noble 1 Step+ Cup (AMT Item Number/ AMT Description): NBCA-13A-B Recalled by...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Check 7 Panel Drug Cup: (AMP/COC/MDMA/MET/OPI/PCP/THC) Recalled by...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ToxCup Drug Screen Cup (AMT Item Number/ AMT Description): HT29A/"ToxCup¿...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UIBC Recalled by Beckman Coulter Inc. Due to The manufacturer has identified...
The Issue: The manufacturer has identified that the use of Unsaturated Iron Binding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Consult Diagnostics Drugs Abuse Test Cup (AMT Item Number/ AMT Recalled by...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Speed Stitch Needle Cassette Recalled by ArthroCare Corporation Due to Due...
The Issue: Due to a supplier error where a portion of the raw material was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tranexamic Acid Injection Recalled by Mylan Institutional LLC Due to...
The Issue: Labeling: Label Mix-Up; potential for cartons labeled as Tranexamic Acid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amiodarone Hydrochloride Injection Recalled by Mylan Institutional LLC Due...
The Issue: Labeling: Label Mix-Up; potential for cartons labeled as Tranexamic Acid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Goldenseal Root Powder Organic Recalled by Maison Terre, LLC Due to...
The Issue: Microbial Contamination of Non-Sterile Products: FDA laboratory analysis...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%) Recalled by...
The Issue: Chemical Contamination: FDA analysis found the product contains methanol,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%) Recalled by...
The Issue: CGMP Deviations: All other lots are being recalled because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SkinGuard 24 All-Day Hand Sanitizer 8 oz. bottle with foam pump Recalled by...
The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Skin Guard 24 All-Day Hand Sanitizer 1 4"x6" Hand Sanitizing Recalled by...
The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Skin Guard 24 All-Day Hand Sanitizer 10 mL Pocket Pen Dist by: SG24 LLC...
The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SkinGuard 24 All-Day Hand Sanitizer 2.67 oz. bottle with foam pump Recalled...
The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine HCl Injection Recalled by Hikma Pharmaceuticals USA Inc. Due...
The Issue: Sub-potent Drug: Out-of-Specification assay results found at 3 month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NM/CT 870 DR Model # H3100AS Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM670 Pro Model # H3100XB Recalled by GE Healthcare, LLC Due to...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM 630 Model # H3101RH Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.