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. 2,693 recalls have been distributed to Minnesota in the last 12 months.
Showing 1941–1960 of 29,186 recalls
Recalled Item: BD Pyxis MedBank CUBIE Replenishment Station Product / Material ID Recalled...
The Issue: Due to a software issue, when attempting to restock the automated dispensing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0 Recalled by...
The Issue: Nerve Monitoring System with certain software versions has potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DXR System Recalled by Philips North America Llc Due to Potential...
The Issue: Potential for collimator to fall as a result of incorrect installation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VH-3010 Power Supply. Used to deliver power to the Recalled by Maquet...
The Issue: Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DXR System Recalled by Philips North America Llc Due to Potential...
The Issue: Potential for collimator to fall as a result of incorrect installation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLX/TLC SP Guided Implant Driver Recalled by Straumann USA LLC Due to The...
The Issue: The devices are missing the laser marked depth markings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS¿PLUS¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1¿MP Recalled by Ethicon Endo...
The Issue: Identified curing issues with the silicone during the needles manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLENE BLU 18IN(45CM) USP6-0(M0.7) S/A P-1 PRM Recalled by Ethicon Endo...
The Issue: Identified curing issues with the silicone during the needles manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH Recalled by Ethicon Endo...
The Issue: Identified curing issues with the silicone during the needles manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDSII¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1 Recalled by Ethicon Endo Surgery,...
The Issue: Identified curing issues with the silicone during the needles manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venue Go Models: R2 (Model Number H45181VG) Recalled by GE Medical Systems,...
The Issue: The battery for certain ultrasound systems can potentially develop an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venue Fit Models: R3 (Model Number H45303VFSC Recalled by GE Medical...
The Issue: The battery for certain ultrasound systems can potentially develop an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Blueprint Mixed Reality Coracoid Clamp Recalled by Tornier S.A.S....
The Issue: Stryker identified an elevated complaint rate related to difficulties using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Blueprint Mixed Reality Glenoid Digitizer Recalled by Tornier S.A.S....
The Issue: Stryker identified an elevated complaint rate related to difficulties using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Blueprint Mixed Reality Depth Stop Pin Recalled by Tornier S.A.S....
The Issue: Stryker identified an elevated complaint rate related to difficulties using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Blueprint Mixed Reality Instrument Kit Recalled by Tornier S.A.S....
The Issue: Stryker identified an elevated complaint rate related to difficulties using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ReNewal ENT Coblator II PROcise XP Wand Recalled by MEDLINE...
The Issue: Medline ReNewal has identified that the drip chambers of affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Blueprint Mixed Reality Box Base Recalled by Tornier S.A.S. Due to...
The Issue: Stryker identified an elevated complaint rate related to difficulties using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ReNewal Coblator II ENT Evac 70 Xtra HP Recalled by MEDLINE...
The Issue: Medline ReNewal has identified that the drip chambers of affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ReNewal Coblator II Evac 70 Xtra Plasma Wand Recalled by MEDLINE...
The Issue: Medline ReNewal has identified that the drip chambers of affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.