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. 2,257 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,257 in last 12 months

Showing 4018140200 of 47,027 recalls

FoodApril 10, 2014· The Pastene Companies Ltd.

Recalled Item: Pastene ITAL NIDI #81 Recalled by The Pastene Companies Ltd. Due to Semolina...

The Issue: Semolina pasta fails to declare the allergen"wheat"

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 10, 2014· The Pastene Companies Ltd.

Recalled Item: Pastene ITAL TAGLIATELLE VERDI #80 Recalled by The Pastene Companies Ltd....

The Issue: Semolina pasta fails to declare the allergen"wheat"

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 10, 2014· Synthes, Inc.

Recalled Item: Synthes External Fixation Systems (Small Recalled by Synthes, Inc. Due to...

The Issue: Labeling changes have been made related to MR (Magnetic Resonance imaging)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Potential for biased...

The Issue: Potential for biased results when a Multiple Window (MW) code is associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Ortho-Clinical Diagnostics

Recalled Item: enGen Laboratory Automation Systems (enGen) with TCAutomation -- For in...

The Issue: Software anomaly: potential for delay in the reporting of patient sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Potential for biased results when a Multiple Window (MW) code is associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Potential for biased results when a Multiple Window (MW) code is associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems VitD Total 100 test Recalled by Siemens Healthcare...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems VitD 500 test Recalled by Siemens Healthcare...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems TSH3 Ultra Recalled by Siemens Healthcare Diagnostics,...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems BRAHMS PCT 100 test Sold only OUS Recalled by Siemens...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems TSH3 Ultra Ready Pack Recalled by Siemens Healthcare...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems TSH3 Ultra 2500 tests Catalog Number: 04862625...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems VitD 100 test Recalled by Siemens Healthcare...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Naturalyte Liquid Bicarbonate Concentrate Recalled by Fresenius Medical Care...

The Issue: Naturalyte Liquid Bicarbonate maybe contaminated

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

Class I — Serious Health HazardOngoing
DrugApril 9, 2014· Nature's Universe

Recalled Item: THINOGENICS Recalled by Nature's Universe Due to Undeclared Sibutramine

The Issue: Marketed Without an Approved NDA/ANDA: Product contains undeclared sibutramine.

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 9, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Cetirizine Hydrochloride Chewable Tablets Recalled by Caraco Pharmaceutical...

The Issue: Failed Impurities/Degradation Specifications: out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugApril 9, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Children's Cetirizine Hydrochloride Chewable Tablets Recalled by Caraco...

The Issue: Failed Impurities/Degradation Specifications: out of specification results...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 9, 2014· Cochlear Americas Inc.

Recalled Item: Cochlear Baha Soft tissue gauge 6mm. Reusable instrument used to Recalled by...

The Issue: Cochlear America is recalling Cochlear Baha Soft Tissue Gauge due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to When the E-NMT-01 module...

The Issue: When the E-NMT-01 module is used in conjunction with the ElectroSensor, the...

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

Class II — Potential Health HazardOngoing