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. 1,752 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
1,752 in last 12 months

Showing 4336143380 of 52,120 recalls

DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Vitamin B12 Methylcobalamin with MIC Injection USP 1000 mcg/ml Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Vitamin B12 Cyanocobalamin Injection USP 1000 mcg/ml Recalled by Medical...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: MIC Injection USP Recalled by Medical Supply Liquidators Llc Due to Marketed...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: B Complex for Injection USP with Methylcobalamin 1000 mcg/ml Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Vitamin B12 Methylcobalamin Injection USP 1000 mcg/ml Recalled by Medical...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Super MIC B Complex for L-Carnitine for Injection USP with Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Vitamin B12 Methylcobalamin 5000 Injection USP 5000 mcg/ml Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Glutathione Injection USP Recalled by Medical Supply Liquidators Llc Due to...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: BCAA 4% Branched Chain Amino Acid Injection USP Recalled by Medical Supply...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Vitamin B12 Hydroxocobalamin Injection USP 1000 mcg/ml Recalled by Medical...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: G.A.C. 375 Injection USP Recalled by Medical Supply Liquidators Llc Due to...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 24, 2014· Doctor's Best, Inc.

Recalled Item: Doctor's Best Red Yeast Rice 1200 Recalled by Doctor's Best, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis discovered undeclared...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 24, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Sonopet Ultrasonic Surgical System Console Recalled by Stryker Instruments...

The Issue: The firm received complaints regarding insufficient irrigation to the tip of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2014· Invacare Corporation

Recalled Item: MK5 NX Controller--Wheelchair controller Recalled by Invacare Corporation...

The Issue: M41 Powered Wheelchairs received through Invacare Service Parts (ISP) have...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2014· Bard Access Systems

Recalled Item: Bard Peripherally Inserted Central Catheter (PICC) and Dialysis catheter...

The Issue: Potential for inadvertent scalpel stick injury involving the safety scalpel.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Cordis Corporation

Recalled Item: Cordis EMPIRA RX PTCA Dilatation Catheter Recalled by Cordis Corporation Due...

The Issue: The balloon may exhibit resistance to the removal of the balloon cover....

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

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

Recalled Item: SIEMENS ADVIA Centaur CP Immunoassay System BNP kit Recalled by Siemens...

The Issue: Complaints of failed calibration.

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

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

Recalled Item: SIEMENS ADVIA Centaur CP Immunoassay System BNP kit Recalled by Siemens...

The Issue: Complaints of failed calibration.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT: product code 882482 Recalled by Philips Medical Systems...

The Issue: Flat Panel Display (FPD) failed to remain securely locked in the deployed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Cordis Corporation

Recalled Item: Cordis EMPIRA NC RX PTCA Dilatation Catheter Recalled by Cordis Corporation...

The Issue: The balloon may exhibit resistance to the removal of the balloon cover....

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

Class II — Potential Health HazardOngoing