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 26841–26860 of 29,186 recalls
Recalled Item: Four Lead TUR irrigation Set Recalled by Baxter Healthcare Corp. Due to A...
The Issue: A firm's internal investigation led to the discovery of pinholes in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superior Approach Resection Guide Assembly. Indicated for primary Recalled...
The Issue: Biomet has initiated this action following an investigation which identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGFA Digital Radiography X-Ray System DX-D 100 Agfa's DX-D 100 Recalled by...
The Issue: Customers could potentially experience intermittent, unintended and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA Analyzer Pipette Tips used on Tosoh AIA-2000 Recalled by Tosoh Smd Inc...
The Issue: Visual inspection of the pipette tips indicated that some of the tips were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Four Lead Arthroscopic Irrigation Set Recalled by Baxter Healthcare Corp....
The Issue: A firm's internal investigation led to the discovery of pinholes in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comfort brand Ear-Loop Face Mask Recalled by Maytex Corp Due to Recent Lab...
The Issue: Recent Lab testing conducted in March 2013 indicates that the product does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuickDraw Venous Cannula with Insertion Kit. ThruPort Systmes. Models QD22...
The Issue: Edwards is recalling the QuickDraw Venous Cannula due to complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optovue iVue with Normative Database (NDB) with Software Version 3.0...
The Issue: Colors from the NDB comparison for Ganglion Cell Complex thickness in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ iPTH ReadyPack Assay 500 Tests Recalled by Siemens Healthcare...
The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ iPTH ReadyPack Assay 100 Tests Recalled by Siemens Healthcare...
The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canister: CO2 canister with GE part numbers 1407-3200-000 Recalled by GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ iPTH Calibrator 6 pk Recalled by Siemens Healthcare...
The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur iPTH Calibrator 2 pk Recalled by Siemens Healthcare...
The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Delta Vaporizer An anesthetic vaporizer is a device used to Recalled by...
The Issue: It has come to Penlon Ltd's attention of an instance where the installation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AFX" Introducer System Recalled by Endologix Inc Due to...
The Issue: Endologix, Inc. initiated this voluntary recall of certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON 60mm Endoscopic Linear Cutter Reloads Black in Flexible Blister...
The Issue: Ethicon Endo-Surgery is initiating a voluntary worldwide recall for ECHELON...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermo Scientific MAS Bilirubin for Siemens and Dimension Vista Systems...
The Issue: It has been confirmed from in-house testing that Direct Bilirubin (DBIL),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens AXIOM Artis zeego x-ray Recalled by Siemens Medical Solutions USA,...
The Issue: Siemens issued a customer safety notice about the overlay of system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HSV 2 Primers Recalled by Life Technologies Corporation Due to Firm received...
The Issue: Firm received complaints that HSV-2 primers failed to amplify HSV-2 DNA.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Responder 5 is a nurse call communication system that connects Recalled by...
The Issue: A counterfeited electronic component was identified in the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.