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. 2,666 recalls have been distributed to Minnesota in the last 12 months.
Showing 5621–5640 of 29,186 recalls
Recalled Item: Alaris PCA Module 8120 Recalled by CareFusion 303, Inc. Due to Alaris PCA...
The Issue: Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Syringe Module Recalled by CareFusion 303, Inc. Due to Alaris PCA...
The Issue: Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris PCU Recalled by CareFusion 303, Inc. Due to Alaris PCA Module...
The Issue: Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Senhance Surgical System Recalled by Asensus Surgical Inc Due to Asensus...
The Issue: Asensus Surgical has identified a malfunction that has occurred and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Tornier Perform Reversed Augmented Glenoid Lateralized Baseplate...
The Issue: One lot of Tournier Perform Reversed Lateralized Baseplates were found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III Video System Center Model Number CV-190. Intended Recalled by...
The Issue: Certain serial numbers of the CV-190 do not start up properly because parts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptima CMV Quant Assay Recalled by Hologic, Inc. Due to Use of assay along...
The Issue: Use of assay along with plasma specimen may result in error code which would...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Expired product distributed
The Issue: Expired product distributed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BREG WALKER FOLDING WALKER WITH WHEELS Utilized as Recalled by Breg Inc Due...
The Issue: Due to walkers not meeting product specifications. Walkers were manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Acrobat-i Vacuum Stabilizer System Intended for use during...
The Issue: Housing Mount Jaw of these devices breaking during normal use and may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Astral 100 and Astral 150 ventilators Recalled by ResMed Ltd. Due to If...
The Issue: If ventilator is on internal battery, not intended to serve as a primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject(TM) 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack Recalled by...
The Issue: Syringe contains conical tip that is not compatible with certain needleless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***Updated 12/4/23*** (1) Cios Flow (VA30) mobile fluoroscopic C-arm X-ray...
The Issue: Software issue for Cios Alpha, Cios Flow, and Cios Spin VA30 systems,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Cios Alpha (VA30) mobile fluoroscopic C-arm X-ray System Recalled by...
The Issue: Software issue for Cios Alpha, Cios Flow, and Cios Spin VA30 systems,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THUNDERBEAT Recalled by Olympus Corporation of the Americas Due to...
The Issue: Thunderbeats blue seal button may remain in the engaged position after the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: The firm has investigated and confirmed that when DxI 9000 is connected to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THUNDERBEAT Recalled by Olympus Corporation of the Americas Due to...
The Issue: Thunderbeats blue seal button may remain in the engaged position after the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC Plus Aerobic/F Culture Vials Recalled by Becton Dickinson & Co....
The Issue: Certain vials of the BD BACTEC" Plus Aerobic/F Culture Vials have a labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.