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. 2,545 recalls have been distributed to Vermont in the last 12 months.
Showing 1–20 of 27,157 recalls
Recalled Item: EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to...
The Issue: Recall of kits which utilized ChloraPrep Triple Swabsticks from BD. Open or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...
The Issue: The system labeling (user manual and online labeling) did not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artelon FlexBand Dynamic Matrix Recalled by International Life Sciences Due...
The Issue: Augmentation devices failed bacterial endotoxin testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artelon FLEXBAND TWIST .12 3.85x17mm HEX Anchor (Qty Recalled by...
The Issue: Augmentation devices failed bacterial endotoxin testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...
The Issue: The system labeling (user manual and online labeling) did not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...
The Issue: The system labeling (user manual and online labeling) did not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...
The Issue: The system labeling (user manual and online labeling) did not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artelon FlexBand Plus & 41057 Recalled by International Life Sciences Due to...
The Issue: Augmentation devices failed bacterial endotoxin testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Campy CVA Medium 100/PK Recalled by Remel, Inc Due to Customer complaints...
The Issue: Customer complaints report low to no recovery of Campylobacter Jejuni ATCC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: STA Liatest Free Protein S Product Name: STA Recalled by...
The Issue: The potential of out-of-range results and an underestimation of the free...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBA Proton Therapy System - PROTEUS 235 Recalled by Ion Beam Applications...
The Issue: It was identified that eh Universal Beam Triggering Interface (UBTI) is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Recalled by B...
The Issue: The potential for the needle tip to be dull/blunt, difficult to advance,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: B. Braun Product Name: 21GA WINGED INFUSION Recalled by B Braun...
The Issue: The potential for the needle tip to be dull/blunt, difficult to advance,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: B. Braun Product Name: 21GA WINGED INF SET Recalled by B Braun...
The Issue: The potential for the needle tip to be dull/blunt, difficult to advance,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HealthCast "Vital Sync" Remote Patient Monitoring System which consists of:...
The Issue: Due to complaints and investigations stating that alarms from the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxC 700 AU Recalled by Beckman Coulter Mishima K.K. Due to A delay in...
The Issue: A delay in results may occur. When clinical chemistry analyzer calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit:...
The Issue: The instructions for use (IFUs) on specified Cardinal Health Chest Drainage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CHEMISTRY ANALYZER AU5800 Recalled by Beckman Coulter Mishima K.K. Due to A...
The Issue: A delay in results may occur. When clinical chemistry analyzer calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units...
The Issue: Potential for rubber fragment detachment during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units...
The Issue: Potential for rubber fragment detachment during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.