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. 1,016 recalls have been distributed to Tennessee in the last 12 months.
Showing 25021–25040 of 52,000 recalls
Recalled Item: Zilver 635 Biliary Stent 14mm x 40mm Recalled by Cook Medical Incorporated...
The Issue: The instruction for use detail, with respect to removal of the delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver 635 Biliary Stent 5mm x 80mm Recalled by Cook Medical Incorporated...
The Issue: The instruction for use detail, with respect to removal of the delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver 635 Biliary Stent 4mm x 80mm Recalled by Cook Medical Incorporated...
The Issue: The instruction for use detail, with respect to removal of the delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver 635 Biliary Stent 4mm x 80mm Recalled by Cook Medical Incorporated...
The Issue: The instruction for use detail, with respect to removal of the delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levofloxacin Injection in 5% Dextrose Recalled by Baxter Healthcare...
The Issue: Superpotent Drug: High out of specification results for levofloxacin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine 1% + Epinephrine 1:100 Recalled by RXQ Compounding LLC Due to...
The Issue: Subpotent drug: During testing of the retention sample, the firm discovered...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PRO-DEX Surgical Driver Battery Pack PDBP-001 Series PRO-DEX Battery Pack...
The Issue: Visual particulates within a battery Tyvek pouch. The battery is provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 365 Everyday Value Brand White Corn Chips Recalled by Whole Foods Market Due...
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Roche Diagnostics URISYS 1100 Urine Analyzer Part Number: 03617556001...
The Issue: Limits of Detection (LoD) for protein, nitrite, leukocytes, and erythrocytes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Max Instrument Recalled by Becton Dickinson & Co. Due to A trend for...
The Issue: A trend for false positive Candida glabrata results has been confirmed. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Max Instrument Reader Spare Part Recalled by Becton Dickinson & Co. Due...
The Issue: A trend for false positive Candida glabrata results has been confirmed. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exprt Precision System: Revision Hip Recalled by Encore Medical, Lp Due to...
The Issue: Complaints regarding loose proximal body bolts or bolts that were found...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FocalPoint Slide Profiler and BD FocalPoint GS Review Station Recalled by...
The Issue: The device may not function at the lower end (<15 deg. C) of the labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit Recalled by Arrow International Inc Due to...
The Issue: The products labeling contains inconsistencies. In certain instances, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORAIL AMT HIGH OFFSET NECK SEGMENT (KHO) Recalled by DePuy Orthopaedics,...
The Issue: There is the potential for debris/material to be found behind the O-rings in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORAIL AMT COXA VARA NECK SEGMENT (KLA) Pro. Code L20432 Recalled by DePuy...
The Issue: There is the potential for debris/material to be found behind the O-rings in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD) Recalled by DePuy...
The Issue: There is the potential for debris/material to be found behind the O-rings in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StageOne Hip Recalled by Zimmer Biomet, Inc. Due to There is a potential for...
The Issue: There is a potential for comingling of the 43MM and 51 MM molds
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4.5 Recalled by RAYSEARCH LABORATORIES AB Due to Robust...
The Issue: Robust optimization for plans using beam set + background dose is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors Recalled by The...
The Issue: Potential for leaking product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.