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. 2,690 recalls have been distributed to Tennessee in the last 12 months.
Showing 4941–4960 of 29,188 recalls
Recalled Item: The Prestige Coil System is a product family of embolic Recalled by BALT...
The Issue: Discoloration was identified along the delivery pusher which was attributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva Nova. Model (REF) Numbers 781172. Recalled by Philips...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T CX. Model (REF) Numbers 781271 Recalled by Philips North...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T. Model (REF) Numbers 781196 Recalled by Philips North America...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva XR. Model (REF) Numbers 781153 Recalled by Philips North America Due...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Initial system. Model (REF) Numbers 781178. Recalled by Philips...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T CX. Model (REF) Numbers 781262 Recalled by Philips North...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T. Model. (REF) Numbers 781277 Recalled by Philips North America...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera Achieva 1.5T Pulsar. Model (REF) Number 781171. Recalled by Philips...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Conversion. Model (REF) Numbers 781346 Recalled by Philips...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva Nova-Dual. Model (REF) Number 781173. Recalled by...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T. Model (REF) Numbers 781260 Recalled by...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Tornier Perform Reversed Glenoid Press-Fit Short Post Ti6AI4V...
The Issue: The incorrect device is contained in the labeled package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Framegrabber card may not perform as intended. Monitor may show no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Framegrabber card may not perform as intended. Monitor may show no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Disk Bay may not perform as intended. System may stop functioning and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Disk Bay may not perform as intended. System may stop functioning and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Dual In-Line Memory Modules (DIMMs) may not perform as intended. System may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3:1 Dermacarrier Recalled by Zimmer Surgical Inc Due to Due to manufacturing...
The Issue: Due to manufacturing issue, the product is labeled as 3:1 ratio, but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MB215R - MILLS DUROGRIP TC Micro Needle Holder Recalled by Aesculap Inc Due...
The Issue: Needle Holder MB215R was inadvertently distributed as MB362R. Similarly,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.