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. 2,313 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,313 in last 12 months

Showing 3284132860 of 47,027 recalls

FoodFebruary 11, 2016· International Foodsource, LLC

Recalled Item: IFS Club Bag Pistachio Raw Shelled 80% Wholes Net Wt. Recalled by...

The Issue: Raw pistachios may be contaminated with Salmonella which was determined...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 11, 2016· International Foodsource, LLC

Recalled Item: Sam International Bulk Raw Whole Pistachio 80% VP Net Wt. Recalled by...

The Issue: Raw pistachios may be contaminated with Salmonella which was determined...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 11, 2016· International Foodsource, LLC

Recalled Item: IFS Web Bulk Pistachio Raw Shelled 80% Wholes Net Wt. Recalled by...

The Issue: Raw pistachios may be contaminated with Salmonella which was determined...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 11, 2016· Health Matters America, Inc.

Recalled Item: Organic traditions SPROUTED CHIA & FLAX SEED POWDER Recalled by Health...

The Issue: The repacked product has the potential to be contaminated with Salmonella.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 11, 2016· Health Matters America, Inc.

Recalled Item: Organic traditions SPROUTED FLAX SEED POWDER Recalled by Health Matters...

The Issue: The repacked product has the potential to be contaminated with Salmonella.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 11, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Accu-Chek Inform II Base Unit as a part of the Recalled by Roche Diagnostics...

The Issue: Accu-Chek Inform II Base Unit might produce physical transmission errors in...

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

Class II — Potential Health HazardOngoing
DrugFebruary 10, 2016· Pfizer Inc

Recalled Item: Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid Recalled by...

The Issue: Labeling: Label Mix-Up

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 10, 2016· Philips Electronics North America Corporation

Recalled Item: evaluemed Infant Heel Warmer 301-1223 Recalled by Philips Electronics North...

The Issue: eValueMed Infant Heel Warmers and eValueMed Infant Transport Mattresses bear...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2016· Philips Electronics North America Corporation

Recalled Item: eValueMed Infant Transport Mattress 301-1015 Recalled by Philips Electronics...

The Issue: eValueMed Infant Heel Warmers and eValueMed Infant Transport Mattresses bear...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2016· Focus Diagnostics Inc

Recalled Item: Simplexa Group A Strep Direct (MOL2850) with Direct Amplification Disc...

The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Focus Diagnostics Inc

Recalled Item: Simplexa HSV 1&2 Direct (MOL2150) with Direct Amplification Disc (MOL1451...

The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Focus Diagnostics Inc

Recalled Item: Simplexa Flu A/B & RSV Direct (MOL2650) with Direct Amplification Disc...

The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2016· GE Medical Systems, LLC

Recalled Item: LightSpeed Ultra (8-slice MDAS) Recalled by GE Medical Systems, LLC Due to...

The Issue: GE Healthcare has updated the Service Manuals for a number of CT and PET CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: Percutaneous Insertion Tray Recalled by Arrow International, Inc., Division...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· GE Medical Systems, LLC

Recalled Item: Discovery LS Recalled by GE Medical Systems, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has updated the Service Manuals for a number of CT and PET CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: Ultra 8 IAB: 8Fr 40cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· GE Medical Systems, LLC

Recalled Item: LightSpeed 16 (MDAS only Recalled by GE Medical Systems, LLC Due to GE...

The Issue: GE Healthcare has updated the Service Manuals for a number of CT and PET CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2016· GE Medical Systems, LLC

Recalled Item: Discovery ST Recalled by GE Medical Systems, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has updated the Service Manuals for a number of CT and PET CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: Ultra 8 IAB: 8Fr 30cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· GE Medical Systems, LLC

Recalled Item: LightSpeed QX/I (4-slice MDAS) LightSpeed 4.0 CT Scanner System - Recalled...

The Issue: GE Healthcare has updated the Service Manuals for a number of CT and PET CT...

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

Class II — Potential Health HazardOngoing