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. 2,348 recalls have been distributed to Vermont in the last 12 months.
Showing 20441–20460 of 27,157 recalls
Recalled Item: Allura Xper FD20 Biplane OR Table Recalled by Philips Electronics North...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS Allura 9 (biplane) Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNIQ FD Recalled by Philips Electronics North America Corporation Due to The...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS BN/BV3000 Recalled by Philips Electronics North America Corporation...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroVue SC5b-9 Plus EIA (CE-IVD) Recalled by Diagnostic Hybrids, Inc. Due...
The Issue: A component of the kit was found to contain bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroVue CIC-C1q EIA Recalled by Diagnostic Hybrids, Inc. Due to A component...
The Issue: A component of the kit was found to contain bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroVue SC5b-9 Plus EIA (RUO) Recalled by Diagnostic Hybrids, Inc. Due to A...
The Issue: A component of the kit was found to contain bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniPod¿ Recalled by Insulet Corporation Due to Pod's needle mechanism fails...
The Issue: Pod's needle mechanism fails to deploy or there is a delay in the deployment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniPod¿ Recalled by Insulet Corporation Due to Pod's needle mechanism fails...
The Issue: Pod's needle mechanism fails to deploy or there is a delay in the deployment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM locking screw SLF-TPNG with Stardrive Recess 18 mm. Intended Recalled...
The Issue: It was discovered that the above part number and lot of 2.4mm Locking Screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted...
The Issue: The firm has received 15 complaints over ten years related to the connection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: Perfusion scan feature may not be available on machines running software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Computed Tomography X-ray system Recalled by Philips...
The Issue: Perfusion scan feature may not be available on machines running software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: Perfusion scan feature may not be available on machines running software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: Perfusion scan feature may not be available on machines running software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: Perfusion scan feature may not be available on machines running software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage System One S Cycler (High Permeability Hemodialysis System) Model...
The Issue: Ultrafiltration (UF) Volume software error inaccurate fluid removal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage System One S Cycler (High Permeability Hemodialysis System) Model...
The Issue: Ultrafiltration (UF) Volume software error inaccurate fluid removal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT SP Computed Tomography X-ray system Recalled by Philips...
The Issue: Perfusion scan feature may not be available on machines running software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DGDE Recalled by Implant Direct Sybron Manufacturing, LLC Due to Implant...
The Issue: Implant Direct Sybron Manufacturing, LLC is recalling 26 lots of DGDE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.