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. 2,243 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,243 in last 12 months

Showing 4546145480 of 47,027 recalls

FoodAugust 21, 2012· American Licorice Co

Recalled Item: RED VINES Mixed Bites Recalled by American Licorice Co Due to CA Dept. of...

The Issue: CA Dept. of Public Health collected random samples of Red Vines Black...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 21, 2012· American Licorice Co

Recalled Item: Red Vines Black Licorice Twists Recalled by American Licorice Co Due to CA...

The Issue: CA Dept. of Public Health collected random samples of Red Vines Black...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 21, 2012· Remel Inc

Recalled Item: Oxoid Antimicrobial Susceptibility Discs Recalled by Remel Inc Due to The...

The Issue: The firm is recalling the product because the cartridges may contain discs...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2012· Remel Inc

Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...

The Issue: The firm is recalling the product due to some cartridges may contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2012· Vycor Medical, Inc.

Recalled Item: Vycor Medical ViewSite Brain Access System 17mm/ 11mm / 5cm Recalled by...

The Issue: Vycor Medical recalled their VBAS (Vycor Viewsite Brain Access System)...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2012· Ethicon, Inc.

Recalled Item: ETHICON SURGIFLO HEMOSTATIC MATRIX KIT Plus FlexTip with Thrombin...

The Issue: SURGIFLO Hemostatic Matrix Kit & SURGIFLO Hemostatic Matrix Kit with...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2012· Ethicon, Inc.

Recalled Item: ETHICON SURGIFLO HEMOSTATIC MATRIX Distributed by ETHICON ETHICON Recalled...

The Issue: SURGIFLO Hemostatic Matrix Kit & SURGIFLO Hemostatic Matrix Kit with...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2012· Elekta, Inc.

Recalled Item: Oncentra External Beam 4.1. Radiation treatment planning software designed...

The Issue: During the planning process the beam weights can be changed by the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Mobilett Mira. Mobile X-Ray System. Recalled by Siemens Medical...

The Issue: During regular product monitoring, Siemens has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2012· Remel Inc

Recalled Item: Remel Xpect Clostridium difficile Toxin A/B Recalled by Remel Inc Due to The...

The Issue: The firm is recalling the products due to a potential for false negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2012· Remel Inc

Recalled Item: Remel Xpect Clostridium difficile Toxin A/B Recalled by Remel Inc Due to The...

The Issue: The firm is recalling the products due to a potential for false negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2012· Microgenics Corporation

Recalled Item: Thermo Scientific MAS Omni IMMUNE and Omni IMMUNE PRO Recalled by...

The Issue: In house testing confirmed that CK-MS and Insulin claimed in both Omni...

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

Class III — Low RiskOngoing
Medical DeviceAugust 20, 2012· Abbott Vascular

Recalled Item: Armada 35/ Armada 35 LL PTA Catheters. The device is Recalled by Abbott...

The Issue: Abbott Vascular is recalling the Armada 35 and Armada 35 LL PTA Catheters...

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

Class II — Potential Health HazardOngoing
FoodAugust 17, 2012· Protica, Inc

Recalled Item: ProBalance Protein To Go(TM) Recalled by Protica, Inc Due to Product not...

The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 17, 2012· Protica, Inc

Recalled Item: ProBalance Protein To Go(TM) Recalled by Protica, Inc Due to Product not...

The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 17, 2012· Protica, Inc

Recalled Item: Protein Shots Recalled by Protica, Inc Due to Product not sufficiently...

The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 17, 2012· Protica, Inc

Recalled Item: Protein Wave 15 grams of protein Recalled by Protica, Inc Due to Product not...

The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 17, 2012· Vital Signs Colorado Inc.

Recalled Item: Vital Signs Disposable General Purpose 9 French Temperature Probe For...

The Issue: There is a potential for epistaxis during use of the Disposable General...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw The Recalled by...

The Issue: Stryker has received reports from the field indicating that certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw The Recalled by...

The Issue: Stryker has received reports from the field indicating that certain lots of...

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

Class II — Potential Health HazardOngoing