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. 1,056 recalls have been distributed to Tennessee in the last 12 months.
Showing 17021–17040 of 52,000 recalls
Recalled Item: Lake Champlain chocolates - Milk Chocolate Bar Library 1.1 lbs.- Recalled by...
The Issue: Chocolate may contain plastic pieces
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lake Champlain Chocolates - gift basket- BE MINE Recalled by Champlain...
The Issue: Chocolate may contain plastic pieces
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate Selection (Holiday and regular) 1.Holiday Selection label reads in...
The Issue: Chocolate may contain plastic pieces
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gift Baskets 1. Lake Champlain Chocolates - BASKET OF CHEER Recalled by...
The Issue: Chocolate may contain plastic pieces
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lake Champlain chocolates - FIVE STAR BAR 6 PACK - Recalled by Champlain...
The Issue: Chocolate may contain plastic pieces
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lake Champlain chocolates -FIVE STAR BAR FRUIT&NUT Dark chocolate 1.9oz...
The Issue: Chocolate may contain plastic pieces
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lake Champlain chocolates -FIVE STAR BAR GRANOLA Dark Chocolate 1.9oz...
The Issue: Chocolate may contain plastic pieces
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VITROS Chemistry Products VersaTips - Product Usage: used to dispense...
The Issue: A deformity affecting a specific lot of VITROS¿ Chemistry Products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MARQUEE Disposable Core Biopsy Instruments XX.Xcm Recalled by Bard...
The Issue: Due to the Penetration Depth Switch used to select the desired penetration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHYSIO CONTROL LIFEPAK CR2 Defibrillator 3321605-xxx The LIFEPAK CR2...
The Issue: Due to complaints received regarding missing lid magnets which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Injectable CT Port insertion kits - Product Usage: is Recalled by...
The Issue: The 5F Dignity CT Port kits were packaged with the incorrect size port. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Parietex hydrophilic anatomical mesh 15 cm x 10 cm Recalled by...
The Issue: incorrect device is contained in the package. The packaging label indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENROUTE Transcarotid Stent System Recalled by Silk Road Medical Inc Due to...
The Issue: Due to complaints received that the tip/nose cone may detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Natus Manufacturing Limited Due to The external drainage system...
The Issue: The external drainage system failed to meet Pyrogen test requirements for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grasper/Retriever Recalled by Shent USA, Inc. Due to Mislabeling
The Issue: Mislabeled: Devices labeled as catalog #7208 (Grasper/Retriever, Alligator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grasper/Retriever Recalled by Shent USA, Inc. Due to Mislabeling
The Issue: Mislabeled: Devices labeled as catalog #7208 (Grasper/Retriever, Alligator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Clean-Cath Intermittent Catheter Recalled by C.R. Bard, Inc. Due to The...
The Issue: The device catheter tip was cut off (no tip) and the product packaging was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Delta CSF (Cerebro Spinal Fluid) -Flow Control Valves for Recalled...
The Issue: Potential for variation in radiopaque marking visibility under radiographic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Cerebro Spinal Fluid Flow Control Valves and Shunts. STRATA...
The Issue: Potential for variation in radiopaque marking visibility under radiographic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic PS Medical Cerebro Spinal Fluid (CSF)-Flow Control Valves for...
The Issue: Potential for variation in radiopaque marking visibility under radiographic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.