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. 2,478 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,478 in last 12 months

Showing 2652126540 of 29,186 recalls

Medical DeviceJune 25, 2013· Convatec Inc.

Recalled Item: ConvaTec Flexi-Seal SIGNAL Fecal Management System Recalled by Convatec Inc....

The Issue: ConvaTec notified their customers on 6/25/2013 regarding the manufacturing...

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

Class III — Low RiskOngoing
Medical DeviceJune 25, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur HCY Diluent - 10mL Bottle Catalog number 09877493 (124533)...

The Issue: ADVIA Centaur Homocysteine dilution recovery on the diluent identified the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2013· Convatec Inc.

Recalled Item: ConvaTec Flexi-Seal SIGNAL + Recalled by Convatec Inc. Due to ConvaTec...

The Issue: ConvaTec notified their customers on 6/25/2013 regarding the manufacturing...

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

Class III — Low RiskOngoing
Medical DeviceJune 24, 2013· Stelkast Co

Recalled Item: SC2316 Recalled by Stelkast Co Due to The firm became aware of an incident...

The Issue: The firm became aware of an incident relating to a breach of sterility in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Sonopet Ultrasonic Aspirator Console (Console 110V with Pedal & Pole)...

The Issue: A supplied component exhibiting corrosion was built into the power supply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Sonopet Ultrasonic Aspirator Console 5450-852-000 (Console 230V) Product...

The Issue: A supplied component exhibiting corrosion was built into the power supply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Sonopet Ultrasonic Aspirator Console 5450-851-000(Console 100V) Product...

The Issue: A supplied component exhibiting corrosion was built into the power supply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Matrix 5.5.mm Left and Right Coronal Bender Product Usage: Recalled...

The Issue: A complaint was received of the tips of the Matrix 5.5.mm Left and Right...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Internal Vessel Occluder .5mL Product Number: 10-0050 LeGoo is...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel-0.5 mL LeGoo with 3 Cannula Pouch Recalled...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel-0.5 mL LeGoo w/ no Cannula Product...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Internal Vessel Occluder .25mL Product Number: 10-0025 LeGoo is...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Internal Vessel Occluder 2.5mL Product Number: 10-0250 LeGoo is...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Internal Vessel Occluder 10mL Product Number: 10-1000 LeGoo is...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel-1.0 mL LeGoo with 3 Cannula Pouch Recalled...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Internal Vessel Occluder 5mL Product Number: 10-0500 LeGoo is Recalled...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel- 0.5 mL LeGoo with 3 Cannula Recalled by...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Endovascular Occlusion Gel 0.5 mL Product Number: LG50IT LeGoo...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel- 1.0 mL LeGoo w/ no Cannula Recalled by...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel-0.25 mL LeGoo with 3 Cannula Pouch...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing