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. 2,518 recalls have been distributed to Minnesota in the last 12 months.
Showing 20001–20020 of 29,186 recalls
Recalled Item: Vascular Solutions Twin-Pass Dual Access Catheter Recalled by Vascular...
The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascular Solutions Twin-Pass .023" Dual Access Catheter Recalled by Vascular...
The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RTI Surgical Streamline OCT Occipito-Cervico-Thoracic Spinal Rod Recalled by...
The Issue: RTI Surgical Inc. (RTI) is conducting a voluntary recall on two specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 10mL Syringe Luer-Lok Tip Catalog number 301997 The BD Single Use...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 5ml Syringe Luer-Lok" Tip with Blunt Fill Needle 18G Recalled by Becton...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 3ml Syringe Luer-Lok" Tip Catalog 309657 The BD Single Use Recalled by...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 18G Recalled by...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Keystone Dental PrimaConnex¿ Straight Implant TC Recalled by Keystone Dental...
The Issue: Small diameter (SD) cover screw was packaged with the regular diameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm Synapse PACS Recalled by Fujifilm Medical Systems U.S.A., Inc. Due...
The Issue: Image data for a patients image may not be correct
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Chemistry 1 Calibrator The Chemistry 1 Calibrator (KC110B)...
The Issue: Siemens determined that discrepant low calcium recovery of QC and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agee-WristJack¿ Fracture Reduction System Recalled by Hand Biomechanics Lab...
The Issue: A number of Agee WristJack¿ Fracture Reduction Systems have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ex-TEM Assay for ROTEM delta Thromboelastometry System. Art. no.: 503-05 US...
The Issue: Customers complained of low/empty reagent vials.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LipiFlow thermal Pulsation System Recalled by Tearscience, Inc Due to...
The Issue: Complaints related to an error condition occurring during patient treatment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zero-Gravity Radiation Protection System Radiology Personnel protective...
The Issue: Two customer complaints suggest that excessive rotation of the cable in one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ellman A CYNOSURE COMPANY Minor Surgery Bipolar Cable Recalled by Ellman...
The Issue: Mislabeling of the "expiration date". The expiration date on the outer box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Laboratory Automation System (Product Code ENGEN) configured with...
The Issue: Ortho confirmed that it is possible for the mis-association of sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza VB10A Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Software upgrade to eliminate several issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software upgrade to eliminate several issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDPoint 400 Measurement Cartridge Siemens SMN numbers:10329756...
The Issue: Error in the value assignment for the Chloride calibrators in the RAPIDPoint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDPoint 405 Measurement Cartridge Siemens SMN numbers: 10844812...
The Issue: Error in the value assignment for the Chloride calibrators in the RAPIDPoint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.