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. 1,641 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
1,641 in last 12 months

Showing 4430144320 of 47,027 recalls

DrugFebruary 19, 2013· Novartis Consumer Health

Recalled Item: Target Up & Up Recalled by Novartis Consumer Health Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 18, 2013· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: The product is being recall due to the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 18, 2013· Biomerieux Inc

Recalled Item: VITEK 2 60 computer system when equipped with the following Recalled by...

The Issue: There is a potential to link an isolate result to the wrong patient and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· GE Healthcare

Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...

The Issue: Using Merge Exam in single Study Mode may result in Missing Study Record...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Biomerieux Inc

Recalled Item: VITEK 2 XL computer system when equipped with the following Recalled by...

The Issue: There is a potential to link an isolate result to the wrong patient and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Biomerieux Inc

Recalled Item: VITEK 2 Compact computer system when equipped with the following Recalled by...

The Issue: There is a potential to link an isolate result to the wrong patient and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Ge Medical Systems Information T

Recalled Item: Centricity PACS Web Diagnostic (WebDX) by GE Healthcare Dynamic Imaging...

The Issue: It was reported from a complaint that study category labels of "Prior" and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Ge Healthcare It

Recalled Item: Imagecast PACS with Centricity RIS-IC versions prior to 10.6 Update Recalled...

The Issue: A software defect was discovered that causes images to be out of context...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2013· Moller Vital

Recalled Item: Molift Smart 150 Recalled by Moller Vital Due to The leg spreading mechanism...

The Issue: The leg spreading mechanism will fail to hoist and collapse if assemble...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2013· Moller Vital

Recalled Item: Molift Smart 150 Recalled by Moller Vital Due to The leg spreading mechanism...

The Issue: The leg spreading mechanism will fail to hoist and collapse if assemble...

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

Class II — Potential Health HazardOngoing
DrugFebruary 15, 2013· Warner Chilcott Company LLC

Recalled Item: Femhrt (norethindrone acetate and ethinyl estradiol) tablets Recalled by...

The Issue: Chemical contamination: Firm's inspection discovered the presence of...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2013· Dr Reddys Laboratories Tennessee LLC

Recalled Item: Amoxicillin for Oral Suspension Recalled by Dr Reddys Laboratories Tennessee...

The Issue: Microbial Contamination of Non-Sterile Products: Suspensions made from these...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2013· Hospira Inc.

Recalled Item: METRONIDazole Injection Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: There is the potential for the solution to...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2013· Warner Chilcott Company LLC

Recalled Item: Femhrt (norethindrone acetate and ethinyl estradiol) tablets Recalled by...

The Issue: Chemical contamination: Firm's inspection discovered the presence of...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2013· Warner Chilcott Company LLC

Recalled Item: Jevantique (norethindrone acetate and ethinyl estradiol) tablets Recalled by...

The Issue: Chemical contamination: Firm's inspection discovered the presence of...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 15, 2013· Decoty Coffee Company, Inc

Recalled Item: Taco Seasoning Recalled by Decoty Coffee Company, Inc Due to Undeclared...

The Issue: DeCoty Coffee Company of San Angelo, Texas is recalling its 1.25lb and...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 15, 2013· Kellogg Company

Recalled Item: Kellogg's Special K Red Berries Recalled by Kellogg Company Due to A limited...

The Issue: A limited amount of Kellogg's Special K, Red Berries is being recalled due...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 15, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 and Ingenuity Computed Tomography X-Ray Systems The Brilliance...

The Issue: This field change order is being released to update software and customer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2013· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX Micros IM2 Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...

The Issue: Horiba Medical is recalling ABX Micros IM2 Data Management System because it...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 14, 2013· Becton Dickinson & Company

Recalled Item: BD Vacutainer C&S Transfer Straw Kit C&S Preservative Plus Urine Tube. 4.0...

The Issue: The BD Vacutainer Urinalysis Transfer Straw Kit #364991, Lot 1335484 has...

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

Class III — Low RiskOngoing