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. 2,503 recalls have been distributed to Vermont in the last 12 months.
Showing 7421–7440 of 27,157 recalls
Recalled Item: Zio AT Clinical Manual Recalled by iRhythm Technologies, Inc. Due to...
The Issue: Ambulatory ECG monitoring system labeling update: 1) Clinically actionable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPEED 9X10X10mm Continuous Compression Implant Recalled by Synthes (USA)...
The Issue: The subject products are being recalled because they contain the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes Hammertoe Continuous Compression Implants Recalled by Synthes...
The Issue: The subject products are being recalled because they contain the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPEEDSHIFT20x20x20 Offset 10mm Implant Drill Kit Recalled by Synthes (USA)...
The Issue: The subject products are being recalled because they contain the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPEED 15X12X12mm Continuous Compression Implant Recalled by Synthes (USA)...
The Issue: The subject products are being recalled because they contain the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GaGa Pro Lighting Equipment Co. Ltd. manufactures Class IV Laser Recalled by...
The Issue: GAGA Pro LLS systems was not in compliance with the FDA's Performance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LumiraDx SARS-CoV-2 Antigen (Ag) Liquid Quality Control Kit Catalog #:...
The Issue: Assigned vial lot numbers for the incorrect type of product. SARS-CoV-2 &...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-C6 Recalled by Hamilton Medical AG Due to Due to a malfunction...
The Issue: Due to a malfunction related to the backlight on the ventilator screen. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model...
The Issue: Due to increase in Li-Ion Battery failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WEB Detachment Controller Recalled by MICROVENTION INC. Due to Detachment...
The Issue: Detachment controller, of an aneurysm embolization system, has an out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GORE CARDIOFORM ASD Occluder. cardiovascular implant. Recalled by W L Gore &...
The Issue: Due to manufacturing records (Release Test Results) indicating "Failed".
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insulin Pump/Model: MiniMed 620G/ MMT-1750 MiniMed 640G/ MMT-1711 Recalled...
The Issue: Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insulin Pump/Model: MiniMed 630G/ MMT-1715 Recalled by Medtronic MiniMed Due...
The Issue: Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex MP Port Titanium Low Profile Implanted Port with 5F Recalled by...
The Issue: Printed Instructions for Use (IFU) not shipped with device. The Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens has become aware of three potential software issues with ARTIS pheno...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Lithium (Li) Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Potential for falsely elevated LITH_2 and Li results on the Atellica CH 930...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Lithium_2 (LITH_2) Recalled by Siemens Healthcare Diagnostics,...
The Issue: Potential for falsely elevated LITH_2 and Li results on the Atellica CH 930...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVP software of the Ivenix Infusion System (IIS) Recalled by Fresenius Kabi...
The Issue: Retroactively reported correction from 2022: A software defect may cause an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prep-Fill Guarded Luer Connector (GLC): a. Part Number 57-400 Recalled by...
The Issue: Blister package had an unsealed edge compromising sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berkeley VC-10 Vacuum Curettage System Recalled by Olympus Corporation of...
The Issue: Update to the Instruction for Use (IFU): Olympus is adding a new warning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.