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. 941 recalls have been distributed to Tennessee in the last 12 months.
Showing 46721–46740 of 52,000 recalls
Recalled Item: TWINFIX Ultra HA 6.5 mm with 2 ULTRABRAID Suture Recalled by Smith & Nephew,...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX Ultra PLLA/HA 6.5 mm with 3 ULTRABRAID Suture Recalled by Smith &...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIORAPTOR 2.9 mm Suture Anchor Recalled by Smith & Nephew, Inc. Endoscopy...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR 2.3 mm Suture Anchor with ULTRABRAID COBRAID Suture Recalled by...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID Suture Recalled by Smith &...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX Ultra PLLA/HA 5.5 mm Suture Anchor with 2 ULTRABRAID Suture Recalled...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX Ultra HA 5.5 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX ULTRA PLLA/HA 5.5 mm Suture Anchor with 3 ULTRABRAID Recalled by...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTOSTEORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...
The Issue: The lot number and/or expiration date may be illegible on the outer plastic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefibre Recalled by Novartis Consumer Health Due to The lot number and/or...
The Issue: The lot number and/or expiration date may be illegible on the outer plastic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...
The Issue: The lot number and/or expiration date may be illegible on the outer plastic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...
The Issue: The lot number and/or expiration date may be illegible on the outer plastic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...
The Issue: The lot number and/or expiration date may be illegible on the outer plastic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Xario XG Diagnostic Ultrasound System SSA-680A Used for routine diagnostic...
The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aplio MX Diagnostic Ultrasound System SSA-780A Used for routine diagnostic...
The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M ESPE Unitek Primary Stainless Steel Crowns (First Primary UL4) Recalled...
The Issue: 3M ESPE is recalling Unitek Primary Stainless Steel Crowns (First Primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xario Diagnostic Ultrasound System SSA-660A Used for routine diagnostic...
The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: nanoPOINT Injector System Recalled by Medicel Ag Due to The...
The Issue: The firm initiated this recall of one lot (121402) of nanoPOINT Injectors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Scotchcast Recalled by 3M Company - Health Care Business Due to 3M is...
The Issue: 3M is conducting a voluntary product recall of selected lots of 3M"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.