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 1961–1980 of 29,186 recalls
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: 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.
Recalled Item: Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID 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: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT...
The Issue: AutoPulse NXT Resuscitation System may not provide adequate chest...
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 COVID-19 2.0 24T Product Name: ID 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: Stimulation RC Clinician Programmer Application Recalled by Medtronic...
The Issue: There is a software issue that can permanently disable communication with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience kits used for various procedures: 1) NAIL PACK Recalled...
The Issue: There is a potential for open/weak seals on purchased breather pouches used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience kits used for various procedures: 1) ED CRASH Recalled...
The Issue: There is a potential for open/weak seals on purchased breather pouches used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: to RES Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to There is a...
The Issue: There is a potential for open/weak seals on purchased breather pouches used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience kits used for various procedures: 1) CW PERI GYN...
The Issue: There is a potential for open/weak seals on purchased breather pouches used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience kits used for various procedures: 1) T&A ENDO PACK...
The Issue: There is a potential for open/weak seals on purchased breather pouches used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience kits used for various procedures: 1) RHINOPLASTY PACK...
The Issue: There is a potential for open/weak seals on purchased breather pouches used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.