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. 2,369 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,369 in last 12 months

Showing 1892118940 of 27,157 recalls

Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T030-000 -30" 20 Drop IV Admin Secondary Set. Packaged in a Tyvek pouch...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T105-000WC IV Set w/2 Y-Sites Recalled by WalkMed Infusion, LLC Due to...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: Spike Set Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T090-000W 90" 20 Drop IV Admin Set w/2 Needlefree Y-Sites Recalled by...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-000F Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: The pump (with cushioning foam inserts) is packaged in a Recalled by WalkMed...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of the Triton...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-120F with 1.2 micron filter and FP Clip. Packaged in a Tyvek pouch...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T090-000 90" 20 Drop IV Admin Set. Packaged in a Tyvek pouch Recalled by...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2016· Cardiovascular Systems Inc

Recalled Item: ViperWire Advance Peripheral Guide Wire Recalled by Cardiovascular Systems...

The Issue: The pouch label was missing the use by date (UBD) of 2018-04.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2016· Biomet, Inc.

Recalled Item: TSP Hip Fracture Plating System device Recalled by Biomet, Inc. Due to...

The Issue: The screw may fracture at the junction of the shaft and the head during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2016· Dako North America Inc.

Recalled Item: Dako HER2 CISH pharmDx Kit Recalled by Dako North America Inc. Due to An...

The Issue: An incorrect HER2 probe concentration was used when producing the probe...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2016· Heartware, Inc.

Recalled Item: HeartWare Ventricular Assist System Controller Product Usage: For use as...

The Issue: Loose connector ports in controller body.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Peripherally Inserted Central Catheters (PICC) Recalled by Angiodynamics...

The Issue: There is a potential for stylet stiffening that is not accurately...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Peripherally Inserted Central Catheters (PICC) Recalled by Angiodynamics...

The Issue: There is a potential for stylet stiffening that is not accurately...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2016· Tosoh Bioscience, Inc.

Recalled Item: Instructions for Use (IFU) for Progesterone 3 Calibrator Set Recalled by...

The Issue: Instructions For Use had incorrect lot number and calibrator values

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJune 7, 2016· Synthes (USA) Products LLC

Recalled Item: Depuy Synthes Trauma- Trochanteric Fixation Nail Advanced (TFNA) Blade/Screw...

The Issue: DePuy Synthes is initiating a voluntary medical device recall due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2016· Stryker Neurovascular

Recalled Item: Target Detachable Coils: TARGET HELICAL NANO 1.5 MM X 1 Recalled by Stryker...

The Issue: Stryker Neurovascular has become aware that some units of Target Nano...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2016· Stryker Neurovascular

Recalled Item: Target Detachable Coils: TARGET HELICAL NANO 1 MM X 2 Recalled by Stryker...

The Issue: Stryker Neurovascular has become aware that some units of Target Nano...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2016· Stryker Neurovascular

Recalled Item: Target Detachable Coils: TARGET 360 NANO 1.5 MM X 3 Recalled by Stryker...

The Issue: Stryker Neurovascular has become aware that some units of Target Nano...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2016· Stryker Neurovascular

Recalled Item: Target Detachable Coils: TARGET 360 NANO 1 MM X 2 Recalled by Stryker...

The Issue: Stryker Neurovascular has become aware that some units of Target Nano...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing