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. 1,023 recalls have been distributed to Vermont in the last 12 months.
Showing 12341–12360 of 27,157 recalls
Recalled Item: ABL90 FLEX Recalled by Radiometer Medical ApS Due to The analyzers fail on...
The Issue: The analyzers fail on S7950 (Range +) QC measurements due to the hemolyzer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 620G Insulin Infusion Pump Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX PLUS Recalled by Radiometer Medical ApS Due to The analyzers fail...
The Issue: The analyzers fail on S7950 (Range +) QC measurements due to the hemolyzer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Pin To Rod Coupling External Fixation System Hoffmann II Recalled by...
The Issue: Pin To Rod Coupling could not clamp the pin and rod as intended
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE MODEL: FreeStyle Comfort Oxygen Concentrator - Product Usage: The...
The Issue: Four units of European version FreeStyle Comfort were distributed in the US,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 630G System with SmartGuard Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 640G Insulin Infusion Pump Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safeline Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safeline Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outlook Safety Infusion System Y-type Blood Set Recalled by B. Braun...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry CardioPhase High Sensitivity C-Reactive Protein (hsCRP)...
The Issue: Atellica and ADVIA hsCRP calibrator accuracy has drifted away from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-PSD Electron Recalled by Angiodynamics, Inc. Due to May result in...
The Issue: May result in readings outside of the expected accuracy range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemLife ECLS Procedure Kit - V24/A17 Recalled by Cardiac Assist, Inc Due...
The Issue: The kit contained a 29Fr ProtekDuo cannula instead of a 24Fr Protek Solo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OARTRAC PROSTATE IMMOBILIZATION ENDORECTAL BALLOON DEVICE KIT Recalled by...
The Issue: May result in readings outside of the expected accuracy range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OARtrac PLUS CLINICAL DETECTOR UNIT Catalog Number: OTS-V2-Plus - Product...
The Issue: May result in readings outside of the expected accuracy range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-PSD HDR Recalled by Angiodynamics, Inc. Due to May result in readings...
The Issue: May result in readings outside of the expected accuracy range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.