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. 2,535 recalls have been distributed to Tennessee in the last 12 months.
Showing 22761–22780 of 29,188 recalls
Recalled Item: ULTRA-FAST FIX Knot Pusher Suture Cutters Product Number: 72201537 Intended...
The Issue: Sterility of device maybe compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac...
The Issue: Complaints with the HVAD Abnormal Power Source Switching.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac...
The Issue: Complaints with the HVAD Discolored and Cracked Driveline Outer Sheath.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit Product...
The Issue: Failures of the splice repair kit if exposed to excessive force.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #: 1101 Recalled by...
The Issue: Complaints with the HVAD Retraction of Pins within the driveline connector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...
The Issue: Complaints with the HVAD Internal Controller Alarm Battery failures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lerner Laboratories Mucolexx Recalled by Richard-Allan Scientific Company...
The Issue: Richard Allan Scientific (RAS) is initiating a recall of Mucolytic agent and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyLink Data Management System Recalled by Siemens Healthcare Diagnostics,...
The Issue: System Limitations and Software Issues related to the following features:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortical Screw for M/DN Intramedullary Fixation. Metaphyseal/Diaphyseal Nail...
The Issue: The entire scope of 4.5mm Cortical Screws listed as compatible with the M/DN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mucolytic Agent 1 pint/473 ml Recalled by Richard-Allan Scientific Company...
The Issue: Richard Allan Scientific (RAS) is initiating a recall of Mucolytic agent and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...
The Issue: HeartWare has received complaints relating to damage or bent connection pins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Alcon Custom Pak. The Alcon Customer Pak is an Recalled by Alcon...
The Issue: The supplier of the Devon Light Glove, a component of the Alcon Custom PAK,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRIT-LINE Blood Chamber- an accessory to the Crit line III- Recalled by...
The Issue: Blood chamber connection leaks during the use of the CRIT-LINE¿ Blood Chamber
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Surgical Kits containing Medtronic Covidien Devon(TM) Light Gloves:...
The Issue: Surgical kits contain Medtronic Covidien Devon(TM) Light Gloves which were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by MRP, LLC dba AMUSA Due to...
The Issue: Incorrect expiration date on label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-fend Recalled by GE Healthcare Due to A potential safety issue due to loss...
The Issue: A potential safety issue due to loss of gas monitoring associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EliteCore Full Core Biopsy Device. EliteCore 18G Recalled by Stryker...
The Issue: Potential for the device cannula to overthrow past the intended length.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision HSI Chronic Catheter Sport Pack w/VenaTrac Stylet 14.5...
The Issue: Catheters may not meet antimicrobial specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome HSI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x Recalled by...
The Issue: Catheters may not meet antimicrobial specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision HSI Chronic Catheter Sport Pack w/VenaTrac Stylet 14.5...
The Issue: Catheters may not meet antimicrobial specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.