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. 2,515 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,515 in last 12 months

Showing 61616180 of 47,027 recalls

DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Natural Eyes Floaters Relief Recalled by Optikem International, Inc. Due...

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
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Natural Eyes Allergy Eyes Relief Recalled by Optikem International, Inc....

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
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Natural Eyes Pink Eye Relief Recalled by Optikem International, Inc. Due...

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
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Natural Eyes Aging Eye Relief Recalled by Optikem International, Inc....

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
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Eye strain Relief Recalled by Optikem International, Inc. Due to Lack of...

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
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Natural Eyes Red Eye Relief Recalled by Optikem International, Inc. Due...

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
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Eye Twitching Relief Recalled by Optikem International, Inc. Due to Lack...

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
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Blur Relief Recalled by Optikem International, Inc. Due to Lack of...

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
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Natural Eyes Dryness Relief Recalled by Optikem International, Inc. Due...

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
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: hyalogic For Dry Eyes Recalled by Optikem International, Inc. Due to Lack of...

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
Medical DeviceFebruary 29, 2024· Beckman Coulter, Inc.

Recalled Item: Beckman Coulter DxI 9000 Access Immunoassay Analyzer is a discrete Recalled...

The Issue: The reason for the recall is the pneumatic tubing used in the analytical...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 29, 2024· Becton Dickinson & Co.

Recalled Item: BD Phoenix Yeast ID Panel is a self-inoculating (when used Recalled by...

The Issue: Esculin, a substrate used in other panels and normally in A16 well, was...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 29, 2024· Becton Dickinson & Co.

Recalled Item: BD Phoenix NMIC-306 Panel is a self-inoculating (when used with Recalled by...

The Issue: Products were found to have confirmed drug cross contamination prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2024· Covidien, LP

Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...

The Issue: The potential for trocar seal disengagement when using mesh products...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2024· Covidien, LP

Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...

The Issue: The potential for trocar seal disengagement when using mesh products...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2024· Covidien, LP

Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...

The Issue: The potential for trocar seal disengagement when using mesh products...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2024· Covidien, LP

Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...

The Issue: The potential for trocar seal disengagement when using mesh products...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2024· Covidien, LP

Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...

The Issue: The potential for trocar seal disengagement when using mesh products...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2024· Covidien, LP

Recalled Item: Covidien Auto Suture" Structural Balloon Trocar Recalled by Covidien, LP Due...

The Issue: The potential for trocar seal disengagement when using mesh products...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2024· Covidien, LP

Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...

The Issue: The potential for trocar seal disengagement when using mesh products...

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

Class II — Potential Health HazardOngoing