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. 2,666 recalls have been distributed to Tennessee in the last 12 months.
Showing 9481–9500 of 52,000 recalls
Recalled Item: buPROPrion Hydrochloride Extended-Release Tablets Recalled by SUN...
The Issue: Failed Dissolution Specifications; during stability testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium Recalled by B. Braun Medical Inc Due to Subpotent: Low...
The Issue: Subpotent: Low anti-factor IIa Potency.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Black Fungus Golden Koi 2.5 oz packages 100 bags per Recalled by AH USA...
The Issue: Product may contain salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: vRad PACS with Mammography Recalled by Virtual Radiologic Corp. Due to The...
The Issue: The error resulted in intermittent failure of current (primary) radiology...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylprednisolone Acetate Injectable Suspension Recalled by Amneal...
The Issue: Labeling: Not Elsewhere Classified; A typographical error was observed in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BioFire Respiratory Panel 2.1 (RP2.1) Recalled by BioFire Diagnostics, LLC...
The Issue: Due to manufacturing issue, panels may result in false negative results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Pneumonia Panel (Pneumo) Recalled by BioFire Diagnostics, LLC Due...
The Issue: Due to manufacturing issue, panels may result in false negative results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 20-in vitro diagnostic use only....
The Issue: Potential to cause biased results in the upper end of the reportable range...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tearaway Introducer Kit Recalled by Galt Medical Corporation Due to Sheath...
The Issue: Sheath introducer assemblies could potentially, due to improper storage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus LS-Manual Defibrillator Recalled by Remote Diagnostic...
The Issue: Defibrillator/pacemaker module (DPM) may encounter a problem causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tearaway Introducer Set Recalled by Galt Medical Corporation Due to Sheath...
The Issue: Sheath introducer assemblies could potentially, due to improper storage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bellavista 1000e Ventilator Recalled by Vyaire Medical Due to Vyaire Medical...
The Issue: Vyaire Medical identified two patient safety risks during the use of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bellavista 1000 Ventilator Recalled by Vyaire Medical Due to Vyaire Medical...
The Issue: Vyaire Medical identified two patient safety risks during the use of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Medical Linear Accelerator (ELMA) included in the below platforms:...
The Issue: A component within a limited number of Elekta Linacs has been realized to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betta Link LG Reusable Fishmouth Guide-Intended for use in soft Recalled by...
The Issue: Drill guides might bend when axial forces are applied by surgeon during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BETTA LINK SR REUSABLE PRONGED GUIDE- Intended for use in Recalled by T.A.G....
The Issue: Drill guides might bend when axial forces are applied by surgeon during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BETTA LINK LG KNOTLESS IMPLANT KIT-Intended for use in soft Recalled by...
The Issue: Drill guides might bend when axial forces are applied by surgeon during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betta Link LG Reusable ProngED Guide - Intended for use Recalled by T.A.G....
The Issue: Drill guides might bend when axial forces are applied by surgeon during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BETTA LINK SR KNOTLESS IMPLANT KIT-Intended for use in soft Recalled by...
The Issue: Drill guides might bend when axial forces are applied by surgeon during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BETTA LINK SR REUSABLE FISHMOUTH GUIDE-Intended for use in soft Recalled by...
The Issue: Drill guides might bend when axial forces are applied by surgeon during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.