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 2901–2920 of 52,120 recalls
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.
Recalled Item: stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide PPSU + Stainless...
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 Check Block Recalled by Tornier...
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 HoloBlueprint Application Recalled by Tornier S.A.S. Due to Stryker...
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 mAx Recalled by MEDLINE INDUSTRIES,...
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 Glenoid Box Lid 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: Gabapentin Capsules Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...
The Issue: Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Capsules Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...
The Issue: Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tolterodine Tartrate Extended-Release Capsules Recalled by The Harvard Drug...
The Issue: Failed Dissolution Specifications: Out of specification results obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Unisom Recalled by Chattem Inc Due to CGMP Deviations: Nitrosamine Drug...
The Issue: CGMP Deviations: Nitrosamine Drug Substance Related Issue impurity above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: InPen smart insulin pen Recalled by Medtronic MiniMed, Inc. Due to Insulin...
The Issue: Insulin pens may have been incorrectly assembled therefore users could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ID NOW Influenza A/B 2 24T Product Name: Recalled by Abbott...
The Issue: the impacted lots have a higher occurrence of invalid rates when compared to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ID NOW RSV 24T Product Name: ID NOW Recalled by Abbott...
The Issue: the impacted lots have a higher occurrence of invalid rates when compared to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ID NOW Influenza A/B 2 24T Product Name: Recalled by Abbott...
The Issue: The impacted lots have a higher occurrence of invalid rates when compared to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.