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 27121–27140 of 27,157 recalls
Recalled Item: 6.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Screw Tulip Recalled by NuVasive Inc Due to The tulip portion of the screw...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5mm x 50mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm x 50mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5mm x 35mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEHC OEC Injection Cable for MedRad Provis V Contrast Injector. Recalled by...
The Issue: GE initiated a correction to the instructions/use due to the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model...
The Issue: Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model...
The Issue: Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various SRI Surgical Disposable Accessory Packs. SRI's Disposable Accessory...
The Issue: Distribution of a product that did not meet specifications. (labeling error)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Precision MPi is an all-digital multipurpose tilt-C x-ray system Recalled...
The Issue: It was discovered that the Remote Touch Panel (RTP) of the GE Precision MPi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Benchmark XT/LT and Discovery XT Model Numbers: N750-BMK-FS Recalled by...
The Issue: Ventana Medical System is initiating the recall of the BenchMark and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TSX-301A/2 Aquilion One CT System. The TSX-30IAl2 is a whole Recalled by...
The Issue: The SureStart function may not operate in the usual manner, and you may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXCELART Vantage Recalled by Toshiba American Medical Systems Inc Due to The...
The Issue: The status display in the sequence queue window may not change from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straight Impactor - Dorado IBC Recalled by SpineFrontier, Inc. Due to During...
The Issue: During two separate occasions an impactor plate on the handle broke off...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.