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. 939 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
939 in last 12 months

Showing 44581–44600 of 53,342 recalls

Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
FoodMay 13, 2014· Us Tov, Inc. Dba U.s. Trading Company

Recalled Item: Dragonfly Brand Crushed Chili Powder Recalled by Us Tov, Inc. Dba U.s....

The Issue: IEH sample of Crushed Chili Powder collected at retail was positive for...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 12, 2014· Microline Surgical, Inc.

Recalled Item: Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips...

The Issue: Potential for the Fenestrated Grasper Tip jaw to break when force is applied...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS (R) Chemistry Products FS Calibrator 1 Recalled by Ortho-Clinical...

The Issue: Calibrator values assigned for the calibrator kit lots were released using a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2014· Toshiba American Medical Systems Inc

Recalled Item: Toshiba Infinix X-Ray Interventional System INFX-8000V/UU. An X-Ray system...

The Issue: Although the Flat Panel Detector (FPD) touch sensor is activated during use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS (R) Chemistry Products Calibrator Kit 17 Recalled by Ortho-Clinical...

The Issue: Calibrator values assigned for the calibrator kit lots were released using a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2014· Microline Surgical, Inc.

Recalled Item: Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips...

The Issue: Potential for the Fenestrated Grasper Tip jaw to break when force is applied...

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

Class II — Potential Health HazardOngoing
DrugMay 12, 2014· John W Hollis Inc

Recalled Item: LIPOTROPIC GOLD Recalled by John W Hollis Inc Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Lack of sterility assurance in compounded...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 12, 2014· John W Hollis Inc

Recalled Item: Papaverine HCl 30 mg Recalled by John W Hollis Inc Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Lack of sterility assurance in compounded...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund