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 24901–24920 of 47,027 recalls
Recalled Item: VPS TipTracker Stylet Accessory Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue(R) Central Venous Catheterization Kit Recalled by Arrow...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous Nerve Block Needle Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SnapLock" Catheter/Syringe Adapter Recalled by Arrow International Inc Due...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 cc Luer-Slip Loss of Resistance Syringe Recalled by Arrow International...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Quad-Lumen Central Venous Catheterization Kit with Blue...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Line Kit with Sharps Safety Features and Maximal Barrier...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximal Barrier Drape Recalled by Arrow International Inc Due to Product...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi-Lumen Central Venous Catheterization Kit Recalled...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spring-Wire Guide Introducer Catheter Assembly Recalled by Arrow...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R)...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hot Smoked Keta Beergarden Salmon Recalled by Seabear Company Due to Mislabeling
The Issue: Products recalled due to water phase salt deviations and mislabeling of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cold Smoked Wild Coho Salmon Lox Recalled by Seabear Company Due to Mislabeling
The Issue: Products recalled due to water phase salt deviations and mislabeling of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kit for the Preparation of Technetium TC-99M Mebrofenin Recalled by...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours...
The Issue: Defective Delivery System: Out of specification for adhesive transfer.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.