Product Recalls in Tennessee

Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,520 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,520 in last 12 months

Showing 2380123820 of 29,188 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· 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· 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· 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: 33CM DORSEY GRASPER FORCEPS Recalled by Stryker Endoscopy Due to 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