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. 2,535 recalls have been distributed to Tennessee in the last 12 months.
Showing 22201–22220 of 29,188 recalls
Recalled Item: 5.0mm Unit Rod 270mm Recalled by Synthes (USA) Products LLC Due to This...
The Issue: This product was produced using a finishing process not identified as part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: -Pipeline Embolization Device -Pipeline Flex Embolization Device The...
The Issue: The firm is recalling Pipeline and Pipeline Flex Embolization Devices from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inserter for Titanium Elastic Nails (TEN) Recalled by Synthes (USA) Products...
The Issue: potential for mechanical failures such as breakage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH + LOMB Biotrue ONEday lenses (nesofilcon A) Recalled by Bausch & Lomb...
The Issue: The firm determined that 25 lots had been manufactured with a minor surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO 400 and AMSCO C Small Steam Sterilizers Recalled by Steris Corporation...
The Issue: In AMSCO Small Steam Sterilizers equipped with the CS-iQ feature, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail CM Long. Intramedullary Fixation Rod. The Zimmer...
The Issue: In about 5% of tested samples, the outer tray was found to be compromised....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novocastra Lyophilized Mouse Monoclonal Antibody CD10 (CD10)....
The Issue: These Lot numbers are not stable up to the expiry date on the product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas b 123 POC system The cobas b 123 POC Recalled by Roche Diagnostics...
The Issue: under specific settings, an issue may occur during simultaneous Sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical LEEP REDIKIT-Used as a surgical preparatory kit for Loop...
The Issue: Kit Label incorrect :Labeled with Lidocaine HCI drug cartridges Lidocaine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX Recalled by AGFA Healthcare Corp. Due to Customers have experienced...
The Issue: Customers have experienced IMPAX CV software, specifically, Demographics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CryoConsole Recalled by Medtronic Inc. Cardiac Rhythm Disease...
The Issue: An issue with a USB memory component contained within a subset of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS iTotal CR (Cruciate Retaining) Knee Replacement System-iTOTAL CR...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConFormis iTotal CR Knee Replacement System- ITOTAL CR - IPOLY Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConFormis iTotal Posterior Stabilized Knee Replacement System- ITOTAL...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS iDuo Bicompartmental Knee Replacement System iDUO G2 Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS Unicondylar Knee Replacement System iUNI G2 Recalled by ConforMIS,...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConFormis iDUO G2 Recalled by ConforMIS, Inc. Due to May contain small...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Cranial Flap Tube Clamp and Crimping Device Product Usage: Recalled...
The Issue: The Synthes Cranial Flap Tube Clamp and Crimping Device for Cranial Tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XiO Radiation Treatment Planning System. Used to create treatment plans...
The Issue: Incorrect Treatment Delivery Using Third Party Fixed Wedges.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS iUNI Unicondylar Knee Replacement System iUNI G2 Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.