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. 2,343 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,343 in last 12 months

Showing 2222122240 of 27,157 recalls

Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Halyard Health

Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...

The Issue: The cuff inflation line may detach from the endotracheal tube during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Halyard Health

Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...

The Issue: The cuff inflation line may detach from the endotracheal tube during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2014· Halyard Health

Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...

The Issue: The cuff inflation line may detach from the endotracheal tube during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to Stryker Endoscopy is recalling...

The Issue: Stryker Endoscopy is recalling Laparoscopic manual instruments and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing