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 26641–26660 of 27,157 recalls
Recalled Item: SARNS FLEXIBLE ARTERIAL CANNULA: 8.0 MM (24 FR) WITH 3/8" CONNECTOR Recalled...
The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPB CATHETER KIT- DR OWEN Product Usage: The Sarns Cardioplegia Recalled by...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-COATED SMALL PATIENT PACK Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARNS HIGH-FLOW AORTIC ARCH CANNULA: 5.2 MM (16 FR) 00 WITH 3/8" CONNECTOR...
The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XC HEART/LUNG PACK W/SX25RX Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUSTOM CPB CATHETER KIT-DR. Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPB CATHETER KIT-DR VANTRIGHT Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPB CATHETER KIT-DR GERHARDT Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYO MN XCOATED 3/8X1/2 AV Product Usage: The Sarns Cardioplegia Recalled by...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARNS FLEXIBLE ARTERIAL CANNULA: 7.3 MM (22 FR) 00 WITH 3/8" CONNECTOR...
The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARNS ANTEGRADE: CARDIOPLEGIA CANNULA: ROOT INFUSION VENT/CATHETER WITH 14-...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand name: RayStation. Generic name: Treatment Planning System. Software...
The Issue: The firm decided to recall when an issue was found with the dose calculation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The product has the Catalogue/Part number 60010. Olympic Cool-Cap System...
The Issue: The Olympic Cool-Cap's Control Module has experienced a frozen screen during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension Vista(R) System B12 Flex(R) Reagent Cartridge (K6442) B12...
The Issue: Siemens Healthcare Diagnostics has confirmed that the presence of Intrinsic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: US-001 Rev A brochure is a two sided tri-fold printed Recalled by...
The Issue: Non-Invasive Monitoring Systems Inc (NIMS) is voluntarily recalling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Brilliance iCT and iCT SP are Computed Tomography X-Ray Recalled by...
The Issue: Philips is issuing a software update (version 3.2.4) to the Brilliance iCT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: USA-002 Rev A brochure is a two sided tri-fold printed Recalled by...
The Issue: Non-Invasive Monitoring Systems Inc (NIMS) is voluntarily recalling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For human...
The Issue: The Beauty Angel was marketed without a 510k.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V Series Patient Monitors Recalled by Mindray DS USA, Inc. d.b.a. Mindray...
The Issue: Mindray has identified two software anomalies contained in the V Series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products Recalled by...
The Issue: Sharp edge on the body/housing of the Lynx TM20 TorqueMaster Low Speed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.