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. 2,257 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,257 in last 12 months

Showing 4038140400 of 47,027 recalls

Medical DeviceMarch 17, 2014· Stryker Communications

Recalled Item: SHAPE ARM Recalled by Stryker Communications Due to During the use of the...

The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Stryker Communications

Recalled Item: SHAPE ARM Recalled by Stryker Communications Due to During the use of the...

The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Stryker Communications

Recalled Item: BAM (SHAPE) ARM Recalled by Stryker Communications Due to During the use of...

The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Stryker Communications

Recalled Item: BAM (SHAPE) ARM Recalled by Stryker Communications Due to During the use of...

The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Stryker Communications

Recalled Item: SHAPE ARM Recalled by Stryker Communications Due to During the use of the...

The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Remel Inc

Recalled Item: Oxoid Legionella Latex Test Recalled by Remel Inc Due to A reagent contained...

The Issue: A reagent contained within the product may return false negative results.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Philips Medical Systems, Inc.

Recalled Item: Digital Diagnost Recalled by Philips Medical Systems, Inc. Due to The...

The Issue: The footboard of Patient support for stitching can be fixed in upper...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Remel Inc

Recalled Item: Oxoid Legionella Pneumo Groups 2-14 Recalled by Remel Inc Due to A reagent...

The Issue: A reagent contained within the product may return false negative results.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Smiths Medical ASD, Inc.

Recalled Item: Smiths Medical HOTLINE¿ Fluid Warming Set L-80. Product Usage: intended...

The Issue: Injection port of the Set may leak blood/ IV fluids from the septum of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Smiths Medical ASD, Inc.

Recalled Item: Smiths Medical HOTLINE¿ Fluid Warming Set L-70. Product Usage: intended...

The Issue: Injection port of the Set may leak blood/ IV fluids from the septum of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· 3M Company - Health Care Business

Recalled Item: 3M" Steri-Vac" Gas Sterilizer/Aerators Recalled by 3M Company - Health Care...

The Issue: Recently, 3M received a single report of a potential exposure to Ethylene...

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

Class II — Potential Health HazardOngoing
DrugMarch 14, 2014· Shire Human Genetic Therapies, Inc.

Recalled Item: VPRIV¿ (velaglucerase alfa for injection) Recalled by Shire Human Genetic...

The Issue: Presence of Particulate Matter; Particulates identified as stainless steel...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 14, 2014· Smiley National Inc

Recalled Item: All Natural Recalled by Smiley National Inc Due to Smiley National is...

The Issue: Smiley National is voluntarily recalling all lots of Bali Kratom 40, XL...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 14, 2014· Smiley National Inc

Recalled Item: Enhanced Maeng Da Leaf Powder Recalled by Smiley National Inc Due to Smiley...

The Issue: Smiley National is voluntarily recalling all lots of Bali Kratom 40, XL...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 14, 2014· Smiley National Inc

Recalled Item: Enhanced Bali Leaf Powder Recalled by Smiley National Inc Due to Smiley...

The Issue: Smiley National is voluntarily recalling all lots of Bali Kratom 40, XL...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 14, 2014· Smiley National Inc

Recalled Item: Natural Bali Kratom 40 Recalled by Smiley National Inc Due to Smiley...

The Issue: Smiley National is voluntarily recalling all lots of Bali Kratom 40, XL...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 14, 2014· Breg Inc

Recalled Item: K-Lite Knee 2 Stays with Visco Recalled by Breg Inc Due to Breg is recalling...

The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2014· Breg Inc

Recalled Item: Economy Elastic Knee Sleeve Open Recalled by Breg Inc Due to Breg is...

The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...

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

Class II — Potential Health HazardOngoing
DrugMarch 13, 2014· Pain Free By Nature

Recalled Item: REUMOFAN PLUS Tablets Recalled by Pain Free By Nature Due to Undeclared...

The Issue: Marketed Without an Approved NDA/ANDA; Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 13, 2014· Medtronic MiniMed Inc.

Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Pumps Recalled by Medtronic...

The Issue: Medtronic is recalling the Medtronic MiniMed Paradigm Insulin Infusion Pumps...

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

Class II — Potential Health HazardOngoing