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. 2,664 recalls have been distributed to Tennessee in the last 12 months.
Showing 11121–11140 of 29,188 recalls
Recalled Item: 9100c NXT system - Product Usage: Device is licensed and Recalled by GE...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A Li-Gator Single Use Laparoscopic Clip Applier Recalled by Genicon, Inc....
The Issue: Device malfunction causing the applier to jam, and clip loading failures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aestiva/5 MRI Anesthesia System - Product Usage: The Aestiva/5 MRI Recalled...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Datex-Ohmeda Aisys CS2 Anesthesia System - Product Usage: is Recalled by...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Datex-Ohmeda Avance CS2 Anesthesia System - Product Usage: intended...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen Recalled by...
The Issue: Instructions for use in the package insert for SARS Antigen FIA test were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Cultura Collection and Transport System Recalled by Merit...
The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Cultura Collection and Transport System Recalled by Merit...
The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MeritMedical Cultura Flex Swab Recalled by Merit Medical Systems, Inc. Due...
The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hurricane RX Biliary Balloon Dilatation Catheter Catalog . M00545890...
The Issue: RX tunnel component (black sheath) may detach from the catheter shaft due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novaplus Monitoriing Electrode with Foam Tape and Sticky Gel - Recalled by...
The Issue: Corrosion could cause performance failures in the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novaplus Monitoriing Electrode with Foam Tape and Sticky Gel - Recalled by...
The Issue: Corrosion could cause performance failures in the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Red Dot Monitoring Electrode with Foam Tape - Product Recalled by 3M...
The Issue: Corrosion could cause performance failures in the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Red Dot Monitoring Electrode with Foam Tape - Product Recalled by 3M...
The Issue: Corrosion could cause performance failures in the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Red Dot Monitoring Electrode with 4mm Adapter - Product Recalled by 3M...
The Issue: Corrosion could cause performance failures in the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Sterilizable Defibrillator Paddles Recalled by Philips North...
The Issue: The periodic Paddle Checks recommended in the Instructions for Use for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Model #65220955 Recalled by Medline Industries Inc Due to Non-sterile...
The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Model #650305414 Recalled by Medline Industries Inc Due to Non-sterile...
The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.