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. 2,478 recalls have been distributed to Minnesota in the last 12 months.
Showing 26701–26720 of 29,186 recalls
Recalled Item: 00597203109 Articular Surface CR ART SURF 34/STRIPE YEL 09 Recalled by...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00595203110 Articular Surface XLPE CR ART SURF 3 Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597504110 Provisional AC ART SURF PROV 56/STR GRN 10 Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597201303 Femur CR POR FM COMP SIZE CML Rx Recalled by Zimmer, Inc. Due to...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597202009 Articular Surface CR ART SURF 12/PURPLE 09 Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597004109 Articular Surface CR ART SURF 56/STRIPE GREEN 9 Recalled by...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597503110 Provisional AC ARTSURF PROV 34/STRIPE YEL10 Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 65597201333 Femur CR POR FEM SURF HDN HATCP CML Recalled by Zimmer, Inc. Due...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597106126 Provisional ALL POLY PAT PROV MICRO SZ 26 Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00595201201 Femur CR-FLEX POR FEM B-L Rx Recalled by Zimmer, Inc. Due to...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597104110 Provisional CR ART SURF PROV 56/STR GRN 10 Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Inc. Cardiac Rhythm Disease Management Due...
The Issue: Medtronic recently identified an issue with a subset of Consulta¿ CRT-P and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Infusor SV and LV Elastomeric Infusion Devices. Indicated...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Regional Analgesia Infusor System with Patient Control....
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Multiday lnfusor Recalled by Baxter Healthcare Corp. Due to Due...
The Issue: Due to an increase in complaints for leaks at the distal male Luer and Luer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Sets The Paradigm infusion sets...
The Issue: Medtronic is recalling the Medtronic MiniMed Paradigm Medtronic is recalling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Infusion Pump- Implantable for the intrathecal...
The Issue: Miscalibrated Fill Level Sensor may affect dosing level
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Basal/Bolus Infusor. Indicated for the intravenous...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Intermate Infusion Pump. Indicated for the intravenous...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Infusion Pump Recalled by Codman & Shurtleff, Inc....
The Issue: Miscalibrated Fill Level Sensor may affect dosing level
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.