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. 2,645 recalls have been distributed to Tennessee in the last 12 months.
Showing 12901–12920 of 29,188 recalls
Recalled Item: GIBSON Healthcare Membrane Extended Recalled by Collagen Matrix Inc Due to...
The Issue: The products may have been packaged with an incorrect Instructions for Use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GIBSON Healthcare Membrane 6-9 Recalled by Collagen Matrix Inc Due to The...
The Issue: The products may have been packaged with an incorrect Instructions for Use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GIBSON Healthcare Membrane 6-9 Recalled by Collagen Matrix Inc Due to The...
The Issue: The products may have been packaged with an incorrect Instructions for Use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GIBSON Healthcare Membrane 6-9 Recalled by Collagen Matrix Inc Due to The...
The Issue: The products may have been packaged with an incorrect Instructions for Use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GIBSON Healthcare Membrane Extended Recalled by Collagen Matrix Inc Due to...
The Issue: The products may have been packaged with an incorrect Instructions for Use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haylard Closed Suction System for Neonates/Pediatrics Recalled by Avanos...
The Issue: Avanos Medical has received reports stating that the central lumen of some 5...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinias DAP Meter Recalled by Shimadzu Medical Systems Due to The DAP meters...
The Issue: The DAP meters were found to be outside of tolerance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Histoplasma Immunodiffusion (ID) Antigen Recalled by Immuno-Mycologics, Inc...
The Issue: False positive results due to potential contamination of reagent.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8mm HTR Sterile Hammer Toe Reaming Kit Recalled by Trilliant Surgical, LLC...
The Issue: The firm has identified that parts from the kit, lot: TSL007202, have the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medacta Shoulder SYSTEM HUMERAL ANATOMICAL METAPHYSIS Recalled by Medacta...
The Issue: Certain lot numbers of the Medacta Humeral Anatomical Cementless Metaphysis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Juno DRF Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to...
The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo EZ Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to...
The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo DRF Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to...
The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to the...
The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ascension¿ Silicone PIP-Silicone PIP Sz 1 Recalled by Integra Lifesciences...
The Issue: Silicone PIP Implant mislabeled as a size 1 implant on the outer packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Healix Knotless ADV BR 4.75 Suture Anchor Recalled by DePuy Mitek, Inc., a...
The Issue: Specific product codes and lots of the Mitek HEALIX ADVANCE" Knotless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Healix Knotless ADV BR 5.5 Suture Anchor Recalled by DePuy Mitek, Inc., a...
The Issue: Specific product codes and lots of the Mitek HEALIX ADVANCE" Knotless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Site~Rite 8 Ultrasound Systems-intended for diagnostic ultrasound imaging of...
The Issue: The indicator may show available charge when the battery is close to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 ANA Screen Control Set Recalled by Bio-Rad Laboratories, Inc....
The Issue: A new lot of ANA screen control and any subsequent control lots are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI SHERIDAN SHERI-BRONCH Endobronchial Tube - Product Recalled by...
The Issue: The tracheal and brochial swivel connectors are incorrectly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.