Product Recalls in Michigan

Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,480 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,480 in last 12 months

Showing 4238142400 of 53,342 recalls

FoodNovember 17, 2014· Karlsburger Foods, Inc.

Recalled Item: Karlsburger Foods Taco Seasoning Recalled by Karlsburger Foods, Inc. Due to...

The Issue: Taco Seasoning has an allergen of milk in the product that is not declared...

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

Class I — Serious Health HazardOngoing
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