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 4741–4760 of 29,186 recalls
Recalled Item: Wash station: M1000 Wash Station Assembly & DITI Slide Recalled by Abbott...
The Issue: Products that were intended for export only which were not approved or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-vitro diagnostic kits: (1) Abbott Vysis MDM2 / CEP 12 FISH Probe Kit...
The Issue: Products that were intended for export only which were not approved or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-vitro diagnostic kits: (1) Abbott Vysis LSI ATM (11q22.3) SpectrmOrange...
The Issue: Products that were intended for export only which were not approved or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microalbumin Calibrator Series (mALB CAL)-IVD used to calibrate the...
The Issue: Microalbumin Calibrator Series, MA1567 & MA2426, is running with a negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microalbumin Calibrator Series (mALB CAL)-IVD to calibrate the Microalbumin...
The Issue: Microalbumin Calibrator Series, MA1567 & MA2426, is running with a negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trumpet Recalled by Technicality Inc. Due to The Ring on the Trump Needle...
The Issue: The Ring on the Trump Needle Guide can detach when excessive pressure is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epix Universal Clip Applier Recalled by Applied Medical Resources Corp Due...
The Issue: Their is the potential that Universal Clip applier may not load clip after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epix Universal Clip Applier Recalled by Applied Medical Resources Corp Due...
The Issue: Their is the potential that Universal Clip applier may not load clip after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 NI/TU Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 4F X 10 CM STD .018 NI/TU Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 NI/TU Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 4F X 10 CM STD .018 SS/PD Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 SS/PD Recalled by Angiodynamics, Inc....
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STIFF .018 NI/TU Recalled by Angiodynamics, Inc....
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 SS/SS Recalled by Angiodynamics, Inc....
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 4F X 10CM STIFF .018 NI/TU ECHO Recalled by Angiodynamics,...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STIFF .018 SS/PD Recalled by Angiodynamics, Inc....
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.