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. 2,295 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,295 in last 12 months

Showing 3658136600 of 47,027 recalls

FoodApril 15, 2015· Reaction Nutrition LLC

Recalled Item: REACTION RECOR: Amino Action- 500g (Cherry Lime) Recalled by Reaction...

The Issue: Work out support nutritional supplements manufactured on shared equipment...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 15, 2015· Reaction Nutrition LLC

Recalled Item: REACTION RECOR: Amino Action- 500g (Glacier Blue) Recalled by Reaction...

The Issue: Work out support nutritional supplements manufactured on shared equipment...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 15, 2015· Reaction Nutrition LLC

Recalled Item: Bio Armor CreaMatrix 306g 60 servings Unflavored Recalled by Reaction...

The Issue: Work out support nutritional supplements manufactured on shared equipment...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 15, 2015· Reaction Nutrition LLC

Recalled Item: REACTION RECOR: Amino Action- 500g (Island Breeze) Recalled by Reaction...

The Issue: Work out support nutritional supplements manufactured on shared equipment...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 15, 2015· Reaction Nutrition LLC

Recalled Item: Bio Armor Carno Pump Plus Electrolytes 40 servings (Blue Raspberry) Recalled...

The Issue: Work out support nutritional supplements manufactured on shared equipment...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast Max Severe Congestion & Cough Recalled by Reckitt Benckiser LLC...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast Max DM Max Recalled by Reckitt Benckiser LLC Due to Labeling:...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 15, 2015· Sandoz, Inc

Recalled Item: Cetirizine HCl Chewable Tablet Recalled by Sandoz, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: An out of specification (OOS)...

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

Class III — Low RiskOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast Max Day Time Severe Cold and Fast-Max Night Recalled by Reckitt...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast Max Day Time Severe Congestion & Cough Night Time Cold & Flu...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast Max Cold Recalled by Reckitt Benckiser LLC Due to Labeling:...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast-Max Cold & Sinus Recalled by Reckitt Benckiser LLC Due to...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast Max Night Time Cold & Flu Recalled by Reckitt Benckiser LLC Due...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity Core 128 Computed Tomography X-ray system...

The Issue: During scans with specific protocol steps, the software unexpectedly sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity Core Computed Tomography X-ray system Recalled...

The Issue: During scans with specific protocol steps, the software unexpectedly sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity CT Computed Tomography X-ray system Recalled by...

The Issue: During scans with specific protocol steps, the software unexpectedly sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Brilliance 64 Computed Tomography X-ray system Recalled...

The Issue: During scans with specific protocol steps, the software unexpectedly sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Halyard Health, Inc

Recalled Item: KimVent Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...

The Issue: The internal blue flapper valve of certain KimVent Turbo-Cleaning Closed...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM ARISTOS FX Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the cable cart and the corrugated hose are unable to move freely, the...

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

Class II — Potential Health HazardOngoing
DrugApril 14, 2015· Actavis Laboratories

Recalled Item: Flurandrenolide Tape Recalled by Actavis Laboratories Due to Subpotent Drug:...

The Issue: Subpotent Drug: Flurandrenolide is subpotent.

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

Class III — Low RiskOngoing
Refund