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. 1,099 recalls have been distributed to Minnesota in the last 12 months.
Showing 13901–13920 of 29,186 recalls
Recalled Item: EQUISTREAM XK Alphacurve Long-Term Hemodialysis Catheter REF/Product...
The Issue: The action is being initiated due to complaints received concerning the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet Recalled by...
The Issue: The action is being initiated due to complaints received concerning the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER Recalled by Bard Peripheral...
The Issue: The action is being initiated due to complaints received concerning the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet Recalled by...
The Issue: The action is being initiated due to complaints received concerning the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Fluoride Tubes for Blood Alcohol determinations Part Number:...
The Issue: Lot has been confirmed to have no additive within the tube. Sample processed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anti-fog solution packaged in a Tyvek peel pouch and it Recalled by Medline...
The Issue: The Anti-Fog Solution may not defog properly due to a degradation in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liberty Cycler Cassettes (a disposable cassette that is intended to Recalled...
The Issue: Additional Instructions: step-by step handling and inserting the cassette...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPi-Sense Guided Coagulation System with Visitrax Recalled by AtriCure, Inc....
The Issue: The sterile package seal for the Epi-Sense Guided Coagulation System may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stratus CS Acute Care cTNI TestPak Recalled by Siemens Healthcare...
The Issue: Potential for increased rate of false positive results and/or increased rate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229036A...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Up (Model #11061610) with syngo.CT software versions VA20A...
The Issue: The potential sporadic performance problems may result in scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DVR Crosslock ePAK Screw Driver Recalled by Zimmer Biomet, Inc. Due to There...
The Issue: There is a potential for weak seals of the sterile packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DVR Crosslock ePAK Depth Gauge Recalled by Zimmer Biomet, Inc. Due to There...
The Issue: There is a potential for weak seals of the sterile packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire Trochar Tip Recalled by Zimmer Biomet, Inc. Due to There is a...
The Issue: There is a potential for weak seals of the sterile packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.All (Model #11061630) Recalled by Siemens Medical Solutions USA,...
The Issue: The potential sporadic performance problems may result in scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.