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. 2,332 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,332 in last 12 months

Showing 2550125520 of 47,027 recalls

DrugJanuary 17, 2018· Magno Humphries Laboratories, Inc

Recalled Item: Senna Laxative (sennosides) tablets Recalled by Magno Humphries...

The Issue: Labeling: Label Mix-Up: Customer complaint received that a bottle labeled as...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 17, 2018· Olympus Corporation of the Americas

Recalled Item: Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R Recalled by...

The Issue: Potential breakage of the endoscope s insertion tube bending section during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2018· Olympus Corporation of the Americas

Recalled Item: Uretero-reno fiberscope URF-P6RP6 Recalled by Olympus Corporation of the...

The Issue: Breakage of the endoscope's insertion tube bending section during surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2018· Olympus Corporation of the Americas

Recalled Item: Uretero-reno fiberscope URF-P6 Recalled by Olympus Corporation of the...

The Issue: Breakage of the endoscope's insertion tube bending section during surgical...

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

Class II — Potential Health HazardOngoing
DrugJanuary 16, 2018· Fresenius Kabi USA, LLC

Recalled Item: Vecuronium bromide for Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Failed impurities/ degradation specifications: Out-of-specification (OOS)...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 16, 2018· Sun Pharmaceutical Industries, Inc.

Recalled Item: DOXOrubicin Hydrochloride Liposome Injection Recalled by Sun Pharmaceutical...

The Issue: Lack Of Assurance Of Sterility

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 15, 2018· Jarrow Formulas Inc

Recalled Item: Jarrow Formulas Liquid L-Carnitine Recalled by Jarrow Formulas Inc Due to A...

The Issue: A higher than normal micro result was found at the six month time point for...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 12, 2018· AuroMedics Pharma LLC

Recalled Item: Levofloxacin in 5% Dextrose Injection Recalled by AuroMedics Pharma LLC Due...

The Issue: Presence of Particulate Matter; contains visible particulate matter...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 12, 2018· International Laboratories, Inc.

Recalled Item: Pravastatin Sodium Tablets Recalled by International Laboratories, Inc. Due...

The Issue: Presence of Foreign Tablets/Capsules: bottles could contain both pravastatin...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 12, 2018· International Laboratories, Inc.

Recalled Item: Pravastatin Sodium Tablets Recalled by International Laboratories, Inc. Due...

The Issue: Presence of Foreign Tablets/Capsules: bottles could contain both pravastatin...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 12, 2018· Beckman Coulter Inc.

Recalled Item: 1) Cytomics FC 500 With CXP Software BECKMAN COULTER 2) Recalled by Beckman...

The Issue: A manufacturing defect on the amplifier board of the Flow Cytometers my...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 12, 2018· Beckman Coulter Inc.

Recalled Item: COULTER EPICS XL Flow Cytometer COULTER EPICS XL-MCL Flow Cytometer Recalled...

The Issue: A manufacturing defect on the amplifier board of the Flow Cytometers my...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 12, 2018· Shimadzu Medical Systems

Recalled Item: Sonialvision Safire II Recalled by Shimadzu Medical Systems Due to When...

The Issue: When selecting serial radiography with a pulse rate of 7.5fps (including...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2018· Hill-Rom, Inc.

Recalled Item: Progressa Bed - AC-powered adjustable hospital bed Recalled by Hill-Rom,...

The Issue: A component used within the braking system may break resulting in one or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2018· Cook Inc.

Recalled Item: MINC Benchtop Incubator (Mini Incubator) catalog (K-MINC-1000) G20079 is a...

The Issue: The temperature of the incubation lids of the MINC Bench top Incubators may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2018· Cook Inc.

Recalled Item: MINC Benchtop Incubator (Mini Incubator) catalog (K-MINC-1000 US) G46022 is...

The Issue: The temperature of the incubation lids of the MINC Bench top Incubators may...

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

Class II — Potential Health HazardOngoing
DrugJanuary 11, 2018· Time-Cap Laboratories, Inc.

Recalled Item: Ibuprofen Tablets USP 800 mg Recalled by Time-Cap Laboratories, Inc. Due to...

The Issue: CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 11, 2018· Time-Cap Laboratories, Inc.

Recalled Item: Ibuprofen Tablets USP 400 mg Recalled by Time-Cap Laboratories, Inc. Due to...

The Issue: CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 11, 2018· Time-Cap Laboratories, Inc.

Recalled Item: Ibuprofen Tablets USP 600 mg Recalled by Time-Cap Laboratories, Inc. Due to...

The Issue: CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 11, 2018· Time-Cap Laboratories, Inc.

Recalled Item: Ibuprofen Tablets USP 600 mg Recalled by Time-Cap Laboratories, Inc. Due to...

The Issue: CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being...

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

Class II — Potential Health HazardOngoing
Refund