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 28541–28560 of 29,186 recalls
Recalled Item: TRESTLE LUXE¿ Anterior Cervical Plating System Recalled by Alphatec Spine,...
The Issue: On May 9th 2012 Alphatec Spine received a complaint which reported that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent...
The Issue: There was an error on the outer labeling of this device. The inner label was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon Medical Imaging system. Product Usage: Horizon Medical Imaging is...
The Issue: There is a potential to save reports in RadReport with an Incorrect Final...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This voluntary medical device correction is related to Alcon products...
The Issue: This medical device correction is related to Alcon products that present a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Getinge Group Pediatric Arterial Cannula Maquet Cardiopulmonary AG...
The Issue: Certain pediatric arterial cannulas may have limited flexibility due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit model 8015 Product Usage: The device is Recalled by...
The Issue: The recall was initiated because the Alaris PC unit model 8015 has a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Volume Viewer Plus 5.x (Advantage Workstation 4.2) Volume...
The Issue: Incorrect views and measurements possible. GE Healthcare became aware of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Seno Advantage 1.x Recalled by GE Healthcare, LLC Due to GE Healthcare...
The Issue: GE Healthcare has become aware of an issue associated with the magnification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Advantage CT/PET Fusion for Advantage Windows Workstation with Volume...
The Issue: GE Healthcare has become aware of a potential safety issue due to incorrect...
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...
The Issue: GE Healthcare has recently become aware of inaccurate Scale factor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Advantage Workstations Recalled by GE Healthcare, LLC Due to...
The Issue: GE Healthcare is informing you of incorrect measurements when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bipolar Forceps model number: S02-XXX Recalled by Stingray Surgical...
The Issue: On 05/23/2012, Stingray Surgical Products, LLC., Boca Raton, FL initiated a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA Esophageal Intubation Detector (EID) Recalled by LMA North America Inc...
The Issue: The recall was initiated because LMANA has received a complaint that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intellispace Portal software. Intellispace Portal is a multimodality thin...
The Issue: Philips is issuing a software update to the Intellispace Portal systems to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Portal software and Extended Brillance Workspace software...
The Issue: The Intellispace Portal software and Extended Brillance Workspace software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments. Integra(TM) Jarit(R)...
The Issue: The Integra(TM) Jarit(R) Take-Apart Laparoscopic Instrument shafts were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CYTO-STAT tetraCHROME CD45- FITC/CD56-RD1/CD19-ECD/CD3-PC5 Recalled by...
The Issue: The recall was initiated because Beckman Coulter has determined that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5mm TI Multiloc Screw Length 28MM-Sterile Expiration: 04/29/2012 .019.028S...
The Issue: Two lots of 4.5mm multi-loc screws were recalled due to incorrect labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD GeneOhm Cdiff Assay Recalled by Becton Dickinson & Co. Due to Leakage in...
The Issue: Leakage in Cepheid SmartCycler reaction tubes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage BNP PN 98000XR Intended to be used as Recalled by Alere San...
The Issue: Certain lots of the affected products may have significantly decreased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.