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. 2,489 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,489 in last 12 months

Showing 2468124700 of 29,186 recalls

Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae 28/38 Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Measurement Clinical Chemistry System RAPIDPoint 500...

The Issue: RAPIDPoint 500 Measurement Cartridges may have an error code one or more...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Three-stage Venous Return Cannulae 28 Fr with 3/8" flare Recalled by...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Venous Return Cannulae 24 Recalled by Terumo Cardiovascular...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Venoatrial Cannulae 36/46 Fr with 1/2" flare or connector Recalled by...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Flexible Aortic Arch Cannula 8.0mm with luer Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Dual-stage Venous Return Cannulae 28/38 Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Two-stage Venous Return Cannulae 32/40 & 36/51 Fr with Recalled by...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 3.0mm Round Fluted Bur Soft Touch Sterile Product Usage: Recalled by...

The Issue: There may be missing notches, partial notches or no notches at all in some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 0.5mm Round Fluted Bur Sterile Product Usage: The devices Recalled...

The Issue: There may be missing notches, partial notches or no notches at all in some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 6.0mm Acorn Bur Sterile Product Usage: The devices are Recalled by...

The Issue: There may be missing notches, partial notches or no notches at all in some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 5.0mm Barrel Bur Sterile Product Usage: The devices are Recalled by...

The Issue: There may be missing notches, partial notches or no notches at all in some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 3.0mm x 3.8mm Neuro Drill Less Aggressive Sterile Product Recalled...

The Issue: There may be missing notches, partial notches or no notches at all in some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 1.3mm Wire Pass Drill Sterile Product Usage: The devices Recalled by...

The Issue: There may be missing notches, partial notches or no notches at all in some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 2.0mm Zyphr Elite Round Fluted Bur Sterile Product Usage: Recalled...

The Issue: There may be missing notches, partial notches or no notches at all in some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 6.0mm Zyphr Elite Round Fluted Bur Sterile Product Usage: Recalled...

The Issue: There may be missing notches, partial notches or no notches at all in some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 4.5mm Round Fluted Bur Aggressive Sterile Product Usage: The...

The Issue: There may be missing notches, partial notches or no notches at all in some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 5.0mm Acorn Bur Sterile Product Usage: The devices are Recalled by...

The Issue: There may be missing notches, partial notches or no notches at all in some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 2.0mm Tapered Round Elite Bur Sterile Product Usage: The Recalled by...

The Issue: There may be missing notches, partial notches or no notches at all in some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 4.0mm x 5.1mm Neuro Drill Soft Touch Sterile Product Recalled by...

The Issue: There may be missing notches, partial notches or no notches at all in some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing