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. 1,712 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
1,712 in last 12 months

Showing 4064140660 of 47,027 recalls

Medical DeviceFebruary 3, 2014· Innovative Sterlization Technologies LLC

Recalled Item: OneTray Sealed Sterilization Containers Product Usage: A rigid sterilization...

The Issue: The wrong sterilization time was on the label. The label lists Steam Gravity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2014· Bock,Otto,Orthopedic Ind,Inc

Recalled Item: Otto Bock Aerial and Aerial Active Wheelchair Cushions. Material numbers:...

The Issue: Otto Bock is recalling all Aerial and Aerial Active Wheelchair Cushions from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2014· Maquet Cardiovascular Us Sales, Llc

Recalled Item: MAQUET PLEGIOX Cardioplegia Heat Exchanger The PLEGIOX Cardioplegia Heat...

The Issue: The MAQUET post-marketing vigilance program has identified a discrepancy...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2014· Hospira Inc.

Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to The connection between...

The Issue: The connection between the beeper subassembly and the pump may fail. The...

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

Class II — Potential Health HazardOngoing
DrugJanuary 31, 2014· American Health Packaging

Recalled Item: HydrOXYzine HCl Tablets Recalled by American Health Packaging Due to Good...

The Issue: Good Manufacturing Practices Deviations: The product has an active...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: SETON PHARMACEUTICALS Fluocinolone acetonide 0.01% Topical Oil (Scalp Oil)...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil (Body Oil) 4 fl....

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· American Health Packaging

Recalled Item: HydrOXYzine HCl Tablets Recalled by American Health Packaging Due to Good...

The Issue: Good Manufacturing Practices Deviations: The product has an active...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: SETON PHARMACEUTICALS Fluocinolone Acetonide 0.01% Oil EAR DROPS Recalled by...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: ROYAL PHARMACEUTICALS DermOtic Oil fluocinolone acetonide 0.01% (Ear Drops)...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil (Scalp Oil)...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: DermOtic Oil (fluocinolone acetonide) 0.01% Ear Drops Recalled by Hill...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: SETON PHARMACEUTICALS Fluocinolone Acetonide 0.01% Topical Oil (Body Oil)...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: ROYAL PHARMACEUTICALS Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: ROYAL PHARMACEUTICALS Derma-Smoothe/FS fluocinolone acetonide 0.01% (Scalp...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 30, 2014· Synthes, Inc.

Recalled Item: Synthes CMF Battery Powered Driver Recalled by Synthes, Inc. Due to The CMF...

The Issue: The CMF Battery Powered Driver graphic case contains outlines of the Battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2014· KCI USA, INC.

Recalled Item: PRE2001: Prevena Incision Management Customizable System Box Product Usage:...

The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2014· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Select 3D Arterial Cannulae. Vented Recalled by Medtronic Inc....

The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2014· KCI USA, INC.

Recalled Item: PRE1055: Prevena Dressing Recalled by KCI USA, INC. Due to Prevena...

The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2014· KCI USA, INC.

Recalled Item: PRE1055US: Prevena Dressing Recalled by KCI USA, INC. Due to Prevena...

The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...

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

Class II — Potential Health HazardOngoing