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 4422144240 of 47,027 recalls

FoodFebruary 25, 2013· American Importing Co, Inc

Recalled Item: Smart Sense Fruit & Granola Trail Mix Recalled by American Importing Co, Inc...

The Issue: American Importing Co., d/b/a Amport Foods is voluntarily recalling a...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 25, 2013· American Importing Co, Inc

Recalled Item: Orchard Reserve Recalled by American Importing Co, Inc Due to American...

The Issue: American Importing Co., d/b/a Amport Foods is voluntarily recalling a...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 25, 2013· American Importing Co, Inc

Recalled Item: Vanilla almond granola Recalled by American Importing Co, Inc Due to...

The Issue: American Importing Co., d/b/a Amport Foods is voluntarily recalling a...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 25, 2013· Baxter Healthcare Corp.

Recalled Item: MiniCap Extended Life PD Transfer Set (6") with Twist Clamp. Recalled by...

The Issue: Labeling Revision: Additional instructions for the use of peritoneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Baxter Healthcare Corp.

Recalled Item: MiniCap Extended Life PD Transfer Set. Product Code 5C4449. intended...

The Issue: Labeling Revision: Additional instructions for the use of peritoneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Baxter Healthcare Corp.

Recalled Item: CAPD Solution Transfer Set with Locking Connector. Product Code: 5C4160....

The Issue: Labeling Revision: Additional instructions for the use of peritoneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Baxter Healthcare Corp.

Recalled Item: MiniCap Extended Life PD Transfer Set Extra Short (4") with Recalled by...

The Issue: Labeling Revision: Additional instructions for the use of peritoneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Nova Biomedical Corporation

Recalled Item: Nova StatStrip Xpress Glu-Test Strips (Glucose test strips) Catalog # 42214...

The Issue: Glucose test strips reports no result message when tested

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Nova Biomedical Corporation

Recalled Item: Nova StatStrip Xpress Glu-Test Strips (Glucose test strips) Catalog #...

The Issue: Glucose test strips reports no result message when tested

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Lifescan Inc

Recalled Item: LifeScan brand OneTouch¿ Select Control Solution Recalled by Lifescan Inc...

The Issue: When OneTouch¿ Ultra and OneTouch¿ Select test strips are tested with Ultra...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Nipro Diagnostics, Inc.

Recalled Item: Duane Reade TRUEtrack monitor kit Recalled by Nipro Diagnostics, Inc. Due to...

The Issue: Meter kit outer boxes containing 10 ct. test strips state incorrect storage...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Lifescan Inc

Recalled Item: LifeScan brand OneTouch¿ Ultra Control Solution Recalled by Lifescan Inc Due...

The Issue: When OneTouch¿ Ultra and OneTouch¿ Select test strips are tested with Ultra...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Symbios Medical Products, LLC

Recalled Item: GOPump Elastometric infusion PumpKit with/ and without accesssories all...

The Issue: Received 2 complaints out of 458 distributed pumps in this lot, where flow...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 24, 2013· Clinical Diagnostic Solutions

Recalled Item: Boule Con-Diff Tri-Level Multi-Parameter Assayed Hematology Control Recalled...

The Issue: Elevated MCV results on the 1311-682, 1311-683, and 1311-684 lots.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Baseplate Impactor Extractor TRIATHLON Instruments....

The Issue: Stryker received reports from the field indicating that the handle detached...

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

Class II — Potential Health HazardOngoing
DrugFebruary 22, 2013· Lupin Pharmaceuticals Inc.

Recalled Item: Ethambutol Hydrochloride Tablets USP Recalled by Lupin Pharmaceuticals Inc....

The Issue: Failed Impurities/Degradation Specifications: This product is being recalled...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 22, 2013· Lion Pavilion Ltd.

Recalled Item: Grassplot Ginger Slice Recalled by Lion Pavilion Ltd. Due to Undeclared Sulfites

The Issue: The product contained undeclared sulfites (735 ppm) based on sampling and...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 22, 2013· The King Arthur Flour Company, Inc.

Recalled Item: King Arthur Unbleached Bread Flour Recalled by The King Arthur Flour...

The Issue: Foreign material

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 22, 2013· The King Arthur Flour Company, Inc.

Recalled Item: King Arthur Unbleached All-Purpose Flour Recalled by The King Arthur Flour...

The Issue: Foreign material

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 22, 2013· Aperio Technologies Inc

Recalled Item: Aperio ScanScope System. Aperio ScanScope Models Recalled by Aperio...

The Issue: Aperio initiated this recall because the User Guides incorrectly state the...

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

Class II — Potential Health HazardOngoing