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. 2,313 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,313 in last 12 months

Showing 3254132560 of 47,027 recalls

Medical DeviceMarch 17, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA CHEMISTRY ENZYMATIC CREATININE_2 Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Advia Chemistry Assay: LDL Cholesterol Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Assays: Triglycerides (TRIG) Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...

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

Class II — Potential Health HazardOngoing
DrugMarch 17, 2016· Impax Laboratories, Inc.

Recalled Item: Fenofibrate Capsules (Micronized) 200 mg Recalled by Impax Laboratories,...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskOngoing
Refund
DrugMarch 17, 2016· Impax Laboratories, Inc.

Recalled Item: Fenofibrate Capsules (Micronized) 134 mg Recalled by Impax Laboratories,...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskOngoing
Refund
FoodMarch 17, 2016· Tri-Union Seafoods, L.L.C dba Chicken of the Sea.

Recalled Item: Chicken of the Sea 5 Oz. Canned Chunk Light Tuna in Water Recalled by...

The Issue: Tri-Union Seafoods LLC is voluntarily recalling a limited amount of Chicken...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 17, 2016· Tri-Union Seafoods, L.L.C dba Chicken of the Sea.

Recalled Item: Chicken of the Sea 5 Oz. Canned Chunk Light Tuna in Oil Recalled by...

The Issue: Tri-Union Seafoods LLC is voluntarily recalling a limited amount of Chicken...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 16, 2016· Bumble Bee Foods LLC

Recalled Item: Bumble Bee Chunk Light Tuna in Water Recalled by Bumble Bee Foods LLC Due to...

The Issue: Bumble Bee Foods is recalling 3 specific codes of canned Chunk Light tuna...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 16, 2016· Bumble Bee Foods LLC

Recalled Item: Bumble Bee Chunk Light Tuna in Water Recalled by Bumble Bee Foods LLC Due to...

The Issue: Bumble Bee Foods is recalling 3 specific codes of canned Chunk Light tuna...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 16, 2016· Bumble Bee Foods LLC

Recalled Item: Bumble Bee Chunk Light Tuna in Oil Recalled by Bumble Bee Foods LLC Due to...

The Issue: Bumble Bee Foods is recalling 3 specific codes of canned Chunk Light tuna...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 16, 2016· Actavis Pharma Inc

Recalled Item: Ciprofloxacin Ophthalmic Solution (0.3% as base) Recalled by Actavis Pharma...

The Issue: Failed Impurities/Degradation Specifications: Firm voluntarily recalled...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 16, 2016· Intuitive Surgical, Inc.

Recalled Item: da Vinci S Surgical System (IS4000) user manual English and Recalled by...

The Issue: Intuitive Surgical has found that the use of instruments other than the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2016· Intuitive Surgical, Inc.

Recalled Item: da Vinci S Surgical System (IS1200/IS2000/IS3000) user manual Recalled by...

The Issue: Intuitive Surgical has found that the use of instruments other than the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2016· Terumo Medical Corporation

Recalled Item: PINNACLE¿ Introducer Sheath PINNACLE PRECISION ACCESS SYSTEM¿ Sheath...

The Issue: Terumo Medical is initiating this recall due to complaints of valve leakage...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Ventlab LLC

Recalled Item: STAT-Check Resuscitation Bag Manual Emergency Resuscitation Bag with Carbon...

The Issue: Stat-check CO2 indicators are non-functional. The indicator is yellow when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Invacare Corporation

Recalled Item: Junction Boxes Recalled by Invacare Corporation Due to The firm recently...

The Issue: The firm recently identified a quality issue with the Junction box used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Invacare Corporation

Recalled Item: Invacare¿ Bariatric Bed with mattress and rails Recalled by Invacare...

The Issue: The firm recently identified a quality issue with the Junction box used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA Duodenovideoscope Olympus TJF Type 160F/VF used with an Recalled...

The Issue: New reprocessing instructions for the Olympus TJF-160/VF duodenoscopes,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Invacare Corporation

Recalled Item: Invacare¿ Foot Section for Semi & Full Electric Beds Recalled by Invacare...

The Issue: The firm recently identified a quality issue with the Junction box used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare System X-ray Tomography Computed : Recalled by Philips...

The Issue: It was discovered the patient support tabletop may fail to move in the...

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

Class II — Potential Health HazardOngoing