Product Recalls in Minnesota
Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,752 recalls have been distributed to Minnesota in the last 12 months.
Showing 43961–43980 of 52,120 recalls
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.
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.
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.
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.
Recalled Item: Cooper Surgical TAMPA CATHETER 5 French 33 cm. Intended for Recalled by...
The Issue: Sterility of the device may be compromised due to unsealed pouch
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: Levocarnitine Solution for injection Recalled by John W Hollis Inc Due to...
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.
Recalled Item: Bystolic (nebivolol) Recalled by Forest Pharmaceuticals Inc Due to Failed...
The Issue: Failed Dissolution Specifications: One lot of product is being voluntarily...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CYANOCOBALAMIN FOR INTRAMUSCULAR OR SUBCUTANEOUS USE ONLY Recalled by John W...
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.
Recalled Item: MIC PLUS B12 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.
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.