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. 2,343 recalls have been distributed to Vermont in the last 12 months.
Showing 21921–21940 of 27,157 recalls
Recalled Item: Ebb Complete Tamponade System Recalled by Clinical Innovations, LLC Due to...
The Issue: Potential for a balloon leak in all lots of (CTS-1000) manufactured since...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Hand-held Barcode Scanner Recalled by Ortho-Clinical Diagnostics Due...
The Issue: In combination with the Batch Programming option (only) for programming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fitness Gear Inversion table (Style STE00059FG or Style STE00118FG) Recalled...
The Issue: Reports of customers falling from the Inversion Table and sustaining...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Recalled by Baxter Corporation Englewood Due to Self-Righting Luer...
The Issue: Self-Righting Luer Tip Caps were manufactured and shipped with a missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portable FAR Infrared Sauna Indications including Recalled by Therasage,...
The Issue: Product distributed without 510(k) approval
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FAR-Infrared Heat Home Sauna Recalled by Therasage, LLC. Due to Product...
The Issue: Product distributed without 510(k) approval
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FAR-Infrared Heat Home Sauna Recalled by Therasage, LLC. Due to Product...
The Issue: Product distributed without 510(k) approval
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lubricated Intubating Stylet 6FR that is inserted into an endotracheal...
The Issue: A small piece of the stylet sheath has the potential to shear off upon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx monitor/defibrillator Models M3535A Recalled by Philips...
The Issue: MRx monitor/defibrillator could reboot at an indeterminate time, potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses...
The Issue: One unit from a demo lot of POWERFLEX PRO PTA Dilatation Catheter was left...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flyte Togas are components of the Stryker Flyte System and Recalled by...
The Issue: A single lot (11121171) of Flyte Toga Peel-away X-Large (catalog number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINAC Accelerators: ARTISTE Recalled by Siemens Medical Solutions USA, Inc...
The Issue: A hardware update to replace the old PCB Assembly, Head Driver-G41 with PCB...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco radiation therapy treatment planning system. The Monaco system is...
The Issue: Incorrect CT to ED when using the Monaco Image Statistics Tool.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Focal Sim radiation therapy treatment planning system Recalled by Elekta,...
The Issue: Incorrect CT to ED when using the Monaco Image Statistics Tool.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEPFLUSH-10 (HEPARIN LOCK FLUSH SOLUTION Recalled by Fresenius Kabi USA, LLC...
The Issue: The lot failed pH specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anti-Lambda APC-H7 Recalled by BD Biosciences, Systems & Reagents Due to Two...
The Issue: Two lots of the Anti-Lambda APC-H7 antibody are contaminated with CD38 antibody.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD8 (Leu-2a) PE (In vitro diagnostic) Recalled by BD Biosciences, Systems &...
The Issue: One lot of CD8 PE is contaminated with CD4 FITC and may cause an unexpected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Electric Pen Drive (EPD) System Recalled by Synthes, Inc. Due to In...
The Issue: In May 2013, the original recall was initiated due to complaints the Hand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zippie Zone Pediatric Rigid Wheelchair Model EIRZ1. Recalled by Sunrise...
The Issue: There is the potential for the height adjustable handle to dislodge due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 10 mL Syringe BD Luer-Lok Tip with Blunt Plastic Cannula Recalled by...
The Issue: The stopper of the 10mL BD Luer-Lok syringe is not properly seated in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.