Product Recalls in Rhode Island

Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,314 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,314 in last 12 months

Showing 3836138380 of 47,970 recalls

FoodNovember 18, 2014· Tastefully Simple, Inc

Recalled Item: Product comes in as part of Fabulous Fudge Gift Box. Recalled by Tastefully...

The Issue: Tastefully Simple is recalling various lots of Cookie & Cream Fudge(Fabulous...

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

Class III — Low RiskOngoing
Refund
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· 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· 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 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
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