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. 2,438 recalls have been distributed to Vermont in the last 12 months.
Showing 13081–13100 of 27,157 recalls
Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex Med 4" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex NL 3" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex Med 3" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex NL 4" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iGUIDE System with software build iGuide 2.2.0 Recalled by Elekta, Inc. Due...
The Issue: Potential for iGUIDE to incorrectly monitor the 3D position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroMist product codes: 36-3310-25 - Product Usage: Electrode...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alpha Conducting solution product codes: 3310-25 ASCR - Product Usage:...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroMist product codes: 36-3310-60 - Product Usage: Electrode...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroMist product codes: 36-3310-04 - Product Usage: Electrode...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alpha Conducting solution product codes:3310-15 ACS - Product Usage:...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual-Sided Interhemispheric Recalled by Ad-Tech Medical Instrument...
The Issue: Supplemental information provided with devices indicates that the subdural...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Depth Electrodes Recalled by Ad-Tech Medical Instrument Corporation Due to...
The Issue: Supplemental information provided with devices indicates that the subdural...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Skull Anchor Bolts Recalled by Ad-Tech Medical Instrument Corporation Due to...
The Issue: Supplemental information provided with devices may indicate that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LSB Style Anchor Bolt. Labeled with the following parts: 13mm Recalled by...
The Issue: On June 12, 2019 Ad-Tech was made aware that on three different occasions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Serrato 9.5mm X 90mm Polyaxial Screw Catalog Number 482619590 Serrato...
The Issue: Discrepant length; Lot B88751 90mm screws were manufactured with a 100mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP Precision Integrated System 120V & LEEP Precision Generator Recalled by...
The Issue: The products' cut, coagulate, or blend function may not operate with the use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.