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. 2,504 recalls have been distributed to Tennessee in the last 12 months.
Showing 26341–26360 of 29,188 recalls
Recalled Item: Synthes Tensioning Device The Synthes Osteogenesis System Recalled by...
The Issue: All lots of the Synthes Tensioning Device were recalled due to the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4 and 2.7 MM Locking Screw SLF-TPNG with T8 Stardrive Recalled by Synthes...
The Issue: Specific lots of the SS 2.4mm and SS 2.7mm Locking Screw (self-tapping) due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "***Flo Trac Sensor Model MHD85***" Sterile Recalled by Edwards...
The Issue: The Edwards Lifesciences FloTrac Sensor is being recalled due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica BIOSYSTEMS Recalled by Leica Biosystems Newcastle Ltd. Due to The...
The Issue: The affected lots of the product may contain a contaminant of fungus that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujinon/Fujifilm Ultrasonic Endoscope Intended to provide ultrasonic images...
The Issue: A limited number of endoscopes were shipped to FMSU-ESD with a manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slipped Capital Femoral Epiphysis System Product Usage: Intended for...
The Issue: There is a possibility for the Guide Wires of the Slipped Capital Femoral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific is initiating a recall removal of the 4.0mm x 15mm size of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Large Buttress Compression Nut For Blade Guide Sleeve TFN The Recalled by...
The Issue: The Large Buttress Compression Nut For Blade Guide Sleeve TFN was recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific is initiating a recall removal of the 4.0mm x 15mm size of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Matrix Threaded Persuader Deformity is a comprehensive thoracolumbar...
The Issue: Synthes became aware that during a procedure using the Matrix Threaded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 2.4 VA-LCP 2 CLMN VLR DSTL Radius PL 7H Recalled by Synthes USA HQ,...
The Issue: The possibility exists that 2.4 mm VA-LCP 2 column distal radius plates from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vertebroplasty Needle Kit 10g Diamond Tip Intended to be used Recalled by...
The Issue: Complaints were received of inconsistencies in the expiration dates shown on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Titanium Cannulated Humeral Nail Intended to aid in the Recalled by...
The Issue: The packaging incorrectly depicts the Synthes Titanium Cannulated Humeral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergetics 25 gauge Soft Tip Cannula Recalled by Synergetics Inc Due to One...
The Issue: One lot of 25 gauge Soft-Tip Disposable Cannulas are co-mingled with 23...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 4.5 mm LCP Curved Condylar Plate Intended for buttressing Recalled...
The Issue: The Synthes 4.5 mm LCP Curved Condylar Plate was recalled because a Straight...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.