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. 2,666 recalls have been distributed to Minnesota in the last 12 months.
Showing 6001–6020 of 52,120 recalls
Recalled Item: EYLEA Recalled by Regeneron Pharmaceuticals Inc Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Complaints of syringe breakage
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: minolira (minocycline hydrochloride) extended-release tablets Recalled by...
The Issue: CGMP Deviation: Discontinuation of the Quality program by manufacturer that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cloderm (clocortolone pivalate) Cream Recalled by EPI Health, LLC Due to...
The Issue: CGMP Deviation: Discontinuation of the Quality program by manufacturer that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: minolira (minocycline hydrochloride) extended-release tablets Recalled by...
The Issue: CGMP Deviation: Discontinuation of the Quality program by manufacturer that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Coviden Monoject 60ml Syringe Luer-Lock Tip-used to inject fluid into...
The Issue: Quarantined product was inadvertently distributed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo ProVue Recalled by Stryker Neurovascular Due to Neurovascular devices...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo Trak 21 Microcatheter Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro .014"guide wire Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DAC 044 115cm Recalled by Stryker Neurovascular Due to Neurovascular devices...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo NXT ProVue 3 x 32 Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo XP ProVue Retriever 4 x 20 Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlowGate2 8F x 85cm Recalled by Stryker Neurovascular Due to Neurovascular...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo Pro 14 Microcatheter Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cascade IOMAX Cortical Module Recalled by Cadwell Industries Inc Due to...
The Issue: There is the potential that an electroneurodiagnostic medical device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURGIFOAM" Absorbable Gelatin Powder Kit Recalled by Ethicon, Inc. Due to...
The Issue: Some applicator tips from these lots had open seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Anti-TG Ab Catalog # L2KTG2 (200 Tests) Recalled by Siemens...
The Issue: The potential for falsely elevated patient sample results when using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Anti-TG Ab Catalog # L2KTG6 (600 Tests) Recalled by Siemens...
The Issue: The potential for falsely elevated patient sample results when using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: muRata Vios Monitoring System Model 2050 Recalled by Murata Vios, Inc. Due...
The Issue: During the set-up and workflow to begin Vios monitoring, it has been noticed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prucka 3 Amplifier Model #P1801PA used with CardioLab AltiX...
The Issue: Capacitors in certain Prucka 3 Amplifiers used with CardioLab / ComboLab...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preview Strep A Recalled by Wondfo USA Co Ltd Due to Wondfo USA has...
The Issue: Wondfo USA has identified unauthorized distribution of the Preview Strep A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.