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 5181–5200 of 29,186 recalls
Recalled Item: (1) CareEvent Recalled by Philips North America Due to Push notifications...
The Issue: Push notifications may fail to send to the user under certain conditions....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EDS 3 CSF External Drainage System Recalled by Natus Medical Incorporated...
The Issue: Sterility assurance cannot be guaranteed for external drainage systems due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Navigation, Inc. Due to Their is the...
The Issue: Their is the potential that the percutaneous pin may have a cross-pin that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-X Rover Mobile X-ray System Recalled by Micro-X Ltd. Due to Mobile...
The Issue: Mobile x-ray system can report and deliver a lower post-exposure mAs value...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Anti-HBs Quantitative Reagent Pack Recalled...
The Issue: Affected lots may experience increased calibration failures or an increase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 4000e Thyroid Uptake Systems- Intended to be used by Recalled by...
The Issue: Spring arm failure with Captus 4000e Thyroid Uptake Systems, can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RibLoc U Plus 90 Instrument PRIMARY GUIDE ASSY Recalled by Acumed LLC Due to...
The Issue: Due to potential breakage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B BR2110X18B...
The Issue: The following was missing from the Contraindications Statement: The AVAPS-AE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Actim PROM dipstik Recalled by ACTIM OY Due to Interference testing has...
The Issue: Interference testing has shown that the presence of personal lubricants in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The device is a mobile x-ray system designed to work Recalled by FUJIFILM...
The Issue: When the key switch is turned on, the exposure conditions are set to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Optetrak 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: Exactech Equinoxe Reverse Shoulder System Recalled by Exactech, Inc. Due to...
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 Novation Hip 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: AcuMatch Hip System Recalled by Exactech, Inc. Due to Exactech has received...
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 Optetrak Logic PS Knee System Recalled by Exactech, Inc. Due to...
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 Vantage Mobile Bearing Tibial Inserts Recalled by Exactech, Inc....
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 Vantage Ankle 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: Access Ultrasensitive Insulin only used on the DxI 9000 Access Recalled by...
The Issue: There is an issue with the Access Ultrasensitive Insulin assay protocol file...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Optetrak Logic Knee System Recalled by Exactech, Inc. Due to...
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 Recalled by Exactech, Inc. Due to Exactech has received 3...
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.