Product Recalls in Vermont
Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,332 recalls have been distributed to Vermont in the last 12 months.
Showing 24481–24500 of 27,157 recalls
Recalled Item: Aplio MX Diagnostic Ultrasound System SSA-780A Used for routine diagnostic...
The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAVIS-EX Recalled by Nidek Inc Due to Under certain circumstances, the Left...
The Issue: Under certain circumstances, the Left eye image may be saved as the Right...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Soft Tissue Retractor Small Extendible. Offset blade facilitates...
The Issue: The small extendible Soft Tissue Retractor was recalled due to locking nut...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00 4309-049-00 Trabecular Metal Reverse Shoulder Glenosphere Distractor Rx...
The Issue: Zimmer is initiating a lot specific recall of the Trabecular Metal" Reverse...
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: 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: 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: 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: 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: 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: 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: 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: Edwards Lifesciences Anastaflo Intravascular Shunt Recalled by Edwards...
The Issue: Edwards Lifesciences is recalling certain lots of the Anastaflo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium Trochanteric Fixation Nail (TFN)System Intended to treat stable and...
The Issue: Two lots of Titanium Trochanteric Fixation Nail (TFN) System are missing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 2.4 mm LC-DCP Plate 6 Holes/51mm Product Usage: Intended Recalled by...
The Issue: A complaint was reported regarding a screw being found in a package labeled...
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 Trochanteric Fixation Nail As part of the Synthes Trochanteric...
The Issue: Certain lots of Trochanteric Fixation Nail were distributed to the field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.