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 7981–8000 of 27,157 recalls
Recalled Item: NIM Vital Patient Interface 4.0 (P/N: NIM4CPB1) NIM with Software version...
The Issue: Software anomaly was identified.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ratcheting Screwdriver Handle Recalled by Tornier, Inc Due to The device is...
The Issue: The device is unable to meet sterilization requirements when sterilized per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM Vital Console 4.0 (P/N: NIM4CM01) NIM with Software version 1.3.2...
The Issue: Software anomaly was identified.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Cap-ONE Biteblock The cap-ONE Biteblock is intended Recalled by Nihon...
The Issue: Due to products being shipped/distributed to customers after the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to The firm...
The Issue: The firm received reports of events related to airway obstruction while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM CONTACT EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to...
The Issue: The firm received reports of events related to airway obstruction while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to The firm...
The Issue: The firm received reports of events related to airway obstruction while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTERGARD Woven Vascular Graft is a woven polyester graft coated Recalled by...
The Issue: Mislabeled: Product labeled as Intergard Woven Straight graft , D: 8 mm, L:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Radiology RA600 Recalled by GE Healthcare, LLC Due to Potential...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer Zero Footprint Client Recalled by GE Healthcare,...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Enterprise Web Recalled by GE Healthcare, LLC Due to Potential...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Cardiology CA1000 Recalled by GE Healthcare, LLC Due to Potential...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS RA1000 Recalled by GE Healthcare, LLC Due to Potential for...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FIRMap" Catheter Recalled by Abbott Due to Incorrect product labeling.
The Issue: Incorrect product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TEG 5000 Functional Fibrinogen Reagent Recalled by Haemonetics Corporation...
The Issue: Due to a shift in the citrated blood range for a normal population, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Wet -Field Eraser Recalled by Beaver Visitec International, Inc. Due to...
The Issue: Boxes labeled as Wet-Field Eraser, 18GA Blunt Tip, 45Deg., were shipped...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-Line ventilator adaptor Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential of reduced oxygenation or pneumothorax/barotrauma to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-Line ventilator adaptor Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential of reduced oxygenation or pneumothorax/barotrauma to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1 Series CX phototherapy units equipped with Daavlin's ClearLink Control...
The Issue: Software issue, resuming an interrupted treatment will result in swap of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4 Series CX phototherapy units equipped with Daavlin's ClearLink Control...
The Issue: Software issue, resuming an interrupted treatment will result in swap of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.