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. 2,489 recalls have been distributed to Minnesota in the last 12 months.
Showing 24381–24400 of 29,186 recalls
Recalled Item: Mindray V21 Recalled by Mindray DS USA, Inc. dba Mindray North America Due...
The Issue: Mindray DS USA Inc. initiated a voluntary field corrective action for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion AirLife Heated Infant Breathing Circuit Product Usage:...
The Issue: The CareFusion AirLife Heated Infant Breathing Circuit is being recalled due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Gender Solution Patello-Femoral Joint (PFJ) System Patello-Femoral...
The Issue: Internal review found that five (5) PFJ implant forgings were identified as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW PLATE 20mm INTERAXIS CHARLOTTE F&A SYSTEM Recalled by Wright Medical...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW 3.5mm PLATE CHARLOTTE F&A SYSTEM Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen...
The Issue: These lots of Agar may have exhibited breakthrough growth of vancomycin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minstrel (with scale) Product Usage: is a mobile passive hoist. Recalled by...
The Issue: ArjoHuntleigh received three reports where the bolt under the scale...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Symbia T Series consists of the T16 Recalled by Siemens Medical...
The Issue: Siemens Medical Solutions USA, Inc. is performing a field correction because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Illumina Worklist Manager (IWM) (software v1.0.15) Recalled by Illumina Inc...
The Issue: A software component of the MiSeqDx instrument, called the Illumina Worklist...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Symbia Intevo series consists of the Intevo 16 Recalled by Siemens...
The Issue: Siemens Medical Solutions USA, Inc. is performing a field correction because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RADIANCE v. 2.4X Recalled by Radiometer America Inc Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Portal (ISP) DX/HX/EX Recalled by Philips Medical Systems...
The Issue: The following software issues have been identified in the affected products....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware of a potential safety issue involving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.