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. 2,322 recalls have been distributed to Vermont in the last 12 months.
Showing 31141–31160 of 47,027 recalls
Recalled Item: BVX-450NR Bovie Precise 360 Handpiece 45cm Recalled by Bovie Medical...
The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVX-330BR Bovie Precise 360 Handpiece 33cm Recalled by Bovie Medical...
The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVX-450BR Bovie Precise 360 Handpiece 45cm Recalled by Bovie Medical...
The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVX-330NR Bovie Precise 360 Handpiece 33cm Recalled by Bovie Medical...
The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Tritest CD3 FITC/CD4 PE/CD45 PerCP (IVD) Recalled by Becton, Dickinson...
The Issue: Internal review found that some vials of CD3/CD4/CD45 state that the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S7 MACH FrameLink. The software application is sent in CD format with an IFU...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FrameLink. The software application is sent in CD format with an IFU...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy Cranial S7. The software application is sent in CD format with an...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fusion ENT Application. The software application is sent in CD Recalled by...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy Spine. The software application is sent in CD format with an IFU...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MACH AxiEM Cranial Treon. The software application is sent in Recalled by...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MACH Cranial Treon. The software application is sent in CD format with an...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diocto Liquid (docusate sodium) 50 mg/5 mL Stool Softener Laxative Recalled...
The Issue: Microbial contamination of Non-Sterile Products; positive findings of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Children's Qnasl 40 mcg (beclomethasone dipropionate) Nasal Aerosol Recalled...
The Issue: Failed Content Uniformity Specifications: out of specification test result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Roche/Hitachi MODULAR Analytics Combination Systems Modular D/P: Clinical...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas p 471 centrifuge unit calculator/data processing module Recalled by...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas p 701 Post-Analytical Unit calculator/data processing module Recalled...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS II Aliquoter System calculator/data processing module Recalled by Roche...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: URISYS 2400 Urine Analyzer Automated Urinalysis System Product Usage: The...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RSD 800 Sorting System calculator/data processing module Recalled by Roche...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.