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. 2,673 recalls have been distributed to Minnesota in the last 12 months.
Showing 5201–5220 of 29,186 recalls
Recalled Item: Exactech Alteon Hip XLE Liner Recalled by Exactech, Inc. Due to Exactech has...
The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Truliant Knee System Recalled by Exactech, Inc. Due to Exactech has...
The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer running software version 1.16 or prior...
The Issue: There are potential performance issues found in the DxI 9000 Access...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe Shoulder System Recalled by Exactech, Inc. Due to Exactech...
The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protege GPS Self-Expanding Peripheral Stent System Recalled by Medtronic...
The Issue: Seal defects could compromise the ability of the product packaging to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (5.4 mm diameter) Model:...
The Issue: Instructions for Use-User Deviations related to the reprocessing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFit F30 Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica HistoCore PEGASUS (PROCESSOR Recalled by LEICA BIOSYSTEMS NUSSLOCH...
The Issue: There is an issue regarding poorly processed and/or damaged biopsy tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFit N20 Nasal Mask and User Guide Recalled by ResMed Ltd. Due to Masks...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard Dressing change kit Recalled by ROi CPS LLC Due to ROi CPS...
The Issue: ROi CPS manufactured and distributed medical convenience kits with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calibration Serum Level 3 - IVD For use as a Recalled by Randox Laboratories...
The Issue: Target for Alkaline Phosphatase (ALP) for the AMP optimized to IFCC 37¿C...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (10 mm diameter) Model:...
The Issue: Instructions for Use-User Deviations related to the reprocessing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFit F20 Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calibration Serum Level 3 CAL2351 Recalled by Randox Laboratories Ltd. Due...
The Issue: CK Total in Calibration Serum Level 3, CAL2351, is running with a positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFit F30i Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirTouch N20 Nasal Mask and User Guide Recalled by ResMed Ltd. Due to Masks...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirTouch F20 Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KeySplint Hard Clear - Indicated for the fabrication of orthodontic Recalled...
The Issue: Keyprint Keysplint Hard Clear 1 kg resin bottles were inadvertently packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFit N10 Nasal Masks and User Guide Recalled by ResMed Ltd. Due to Masks...
The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Valleylab FT10 Recalled by Covidien Due to Due to software issue,...
The Issue: Due to software issue, New systems may exhibit an error which may prohibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.