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. 2,508 recalls have been distributed to Vermont in the last 12 months.
Showing 6801–6820 of 27,157 recalls
Recalled Item: LinkSymphoKnee Distal Femoral Augment - Tilastan - Size. 7-8 Recalled by...
The Issue: Fixation screw was inserted through the wrong side of the augment (distal to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LinkSymphoKnee Distal Femoral Augment - Tilastan - Size 7-8 Recalled by...
The Issue: Fixation screw was inserted through the wrong side of the augment (distal to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precision Delivery Set with Filter Recalled by Quest Medical, Inc. Due to...
The Issue: Delivery Sets may have tubing that could become detached that could result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CENTURION MEDICAL PRODUCTS Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: The kit contained an expired component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short Recalled...
The Issue: Product Mislabeled on the outer bag and inner kit Tyvek header bag
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur XP and ADVIA Centaur XPT Anti-HBe2 (aHBe2) 50T- Recalled by...
The Issue: Anti-HBe2 (aHBe2) interference with the Hepatitis B e Antigen (HBeAg) Assay,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term...
The Issue: Label with the incorrect component listed on the inner kit Tyvek header bag
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Covera Vascular Covered Stent is a flexible Recalled by Bard Peripheral...
The Issue: An increase in the reported complaint rate for inability to deploy was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RipCord Syndesmosis Button Recalled by TriMed Inc. Due to Overly aggressive...
The Issue: Overly aggressive tension on the pull suture, while passing the medial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE UNITE FOOT & ANKLE DRILL BIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The recall is due to observed intra-operative screw failure. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE UNITE FOOT & ANKLE Screw Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The recall is due to observed intra-operative screw failure. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE UNITE FOOT & ANKLE Screw Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The recall is due to observed intra-operative screw failure. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Air-Q3 AirQ3 Standard ILA with Manual Cuff Inflation and GA Recalled by...
The Issue: There is an orogastric (OG) tube size discrepancy between the labeling in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge Flow-e Anesthesia System Recalled by Getinge Usa Sales Inc Due to...
The Issue: Due to a software bug, under certain conditions, pressure cannot be built up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge Flow-c Anesthesia System Recalled by Getinge Usa Sales Inc Due to...
The Issue: Due to a software bug, under certain conditions, pressure cannot be built up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge Flow-i Anesthesia Systems Flow-i C20 Recalled by Getinge Usa Sales...
The Issue: Due to a software bug, under certain conditions, pressure cannot be built up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software : myNeedle Guide 2D license Recalled by Siemens Medical Solutions...
The Issue: In the syngo.CT VA40 and syngo.CT VA50 myNeedle Guide application, the order...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirQ3 Self Pressurizing ILA with Automatic Cuff Inflation and GA Recalled by...
The Issue: There is an orogastric (OG) tube size discrepancy between the labeling in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vasoshield Syringe Packs Recalled by Maquet Cardiovascular, LLC Due to...
The Issue: Ink on the Vasoshield syringe Maquet logo may chip resulting in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemopro 2 with Vasoshield Recalled by Maquet Cardiovascular, LLC Due to...
The Issue: Ink on the Vasoshield syringe Maquet logo may chip resulting in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.