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 4356143580 of 47,027 recalls

DrugApril 30, 2013· King Legacy, a wholly owned subsidiary of Pfizer

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...

The Issue: Subpotent Drug: The products were below specification for potency at the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2013· King Legacy, a wholly owned subsidiary of Pfizer

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...

The Issue: Subpotent Drug: The products were below specification for potency at the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2013· King Legacy, a wholly owned subsidiary of Pfizer

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...

The Issue: Subpotent Drug: The products were below specification for potency at the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2013· King Legacy, a wholly owned subsidiary of Pfizer

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...

The Issue: Subpotent Drug: The products were below specification for potency at the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2013· King Legacy, a wholly owned subsidiary of Pfizer

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...

The Issue: Subpotent Drug: The products were below specification for potency at the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2013· King Legacy, a wholly owned subsidiary of Pfizer

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...

The Issue: Subpotent Drug: The products were below specification for potency at the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2013· King Legacy, a wholly owned subsidiary of Pfizer

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...

The Issue: Subpotent Drug: The products were below specification for potency at the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 29, 2013· Biomet, Inc.

Recalled Item: Biomet Trauma Phoenix Retrograde Femoral Connecting Bolt Trauma Fixation...

The Issue: Biomet Trauma ("Biomet") has initiated a recall of Retrograde Femoral...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2013· Heart Sync, Inc

Recalled Item: Vermed Recalled by Heart Sync, Inc Due to On 4/18/13 HEARTSYNC became aware...

The Issue: On 4/18/13 HEARTSYNC became aware of a recall from their wire/connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2013· Beckman Coulter Inc.

Recalled Item: AU2700 Clinical Chemistry Analyzer AU5400 Clinical Chemistry Analyzer...

The Issue: Beckman Coulter is recalling AU2700/AU2700 Plus & AU5400 Clinical Chemistry...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2013· Heart Sync, Inc

Recalled Item: Heart Sync C100-Physio Radiotransparent Defibrillation Electrodes Monophasic...

The Issue: On 4/18/13 HEARTSYNC became aware of a recall from their wire/connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2013· Cardio Medical Products

Recalled Item: Cardio Medical Products Recalled by Cardio Medical Products Due to Covidien...

The Issue: Covidien received customer reports of Arcing/Sparking on the defibrillation...

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

Class II — Potential Health HazardOngoing
DrugApril 26, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Amoxicillin for Oral Suspension Recalled by Teva Pharmaceuticals USA, Inc....

The Issue: Discoloration: This recall is being carried out due to a yellow to brown...

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

Class III — Low RiskOngoing
Refund
FoodApril 26, 2013· Conagra Inc

Recalled Item: Orville Redenbacher's Classic Kettle Korn Recalled by Conagra Inc Due to...

The Issue: The kettle korn flavored ready-to-eat popcorn product may contain...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 25, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: B-CrossLaps/serum (B-CTx in serum) 160 100 tests Immunoassay Recalled by...

The Issue: Roche Diagnostics internal investigations in R&D have shown that the claims...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Leibel-Flarsheim Company LLC

Recalled Item: Hydra Vision DR 60/80 System Recalled by Leibel-Flarsheim Company LLC Due to...

The Issue: A complaint was received in which a hospital physicist indicated the dosage...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· The Anspach Effort, Inc.

Recalled Item: ******iMRI Handpiece. Use with iMRI System Only***Rx Only***Manufacturer:...

The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· The Anspach Effort, Inc.

Recalled Item: ******Swivel/Angle Motor Assembly***Rx Only***The Anspach Effort Recalled by...

The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· The Anspach Effort, Inc.

Recalled Item: ******XMax Handpiece***Rx Only***Manufacturer: The Anspach Effort Recalled...

The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension(R) TACR Flex(R) reagent cartridge (DF107) The TACR method is...

The Issue: Siemens has confirmed that the TACR method may demonstrate reduced on-board...

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

Class II — Potential Health HazardOngoing