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. 2,439 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,439 in last 12 months

Showing 3872138740 of 52,120 recalls

Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Advanced Sterilization Products

Recalled Item: CIDEX Activated Dialdehyde Solution Recalled by Advanced Sterilization...

The Issue: Advanced Sterilization Products (ASP) is recalling the CIDEX Activated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Sunrise Medical (US) LLC

Recalled Item: Quickie IRIS Wheelchair. model EIZ4-2 in combination with option code...

The Issue: Quickie IRIS and Zippie IRIS tilt-in-space wheelchairs with MONO Backrest...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Trumpf Medical Systems, Inc.

Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...

The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Trumpf Medical Systems, Inc.

Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...

The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...

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

Class II — Potential Health HazardOngoing
DrugJuly 27, 2015· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for z-statistic related to...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 27, 2015· Bruce Foods Corporation

Recalled Item: THE ORIGINAL CHICKEN FRY MIX FROM THE MAKERS OF LOUISIANA BRAND HOT SAUCE...

The Issue: Products may be contaminated with peanut protein.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 27, 2015· Christie Cookie Co Inc

Recalled Item: Doubletree Cookie Dough Recalled by Christie Cookie Co Inc Due to Reports of...

The Issue: Reports of clear and green plastic pieces in cookies.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 27, 2015· Bruce Foods Corporation

Recalled Item: LOUISIANA CHICKEN WING SEASONING Recalled by Bruce Foods Corporation Due to...

The Issue: Products may be contaminated with peanut protein.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 27, 2015· Bruce Foods Corporation

Recalled Item: "LOUISIANA" WING KIT containing CHICKEN WING SEASONING Recalled by Bruce...

The Issue: Products may be contaminated with peanut protein.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2015· Ucb, Inc

Recalled Item: univasc (moexipril HCl) tablets Recalled by Ucb, Inc Due to Failed...

The Issue: Failed Dissolution Testing: Failed 24 month dissolution testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2015· Shionogi Inc.

Recalled Item: Nisoldipine Extended Release Tablets Recalled by Shionogi Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJuly 24, 2015· Teva Pharmaceuticals USA

Recalled Item: ADRUCIL (fluorouracil injection Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Presence of Particulate Matter: silcone rubber and fluorouracil crystals...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 24, 2015· Boehringer Ingelheim Roxane Inc

Recalled Item: COMBIVENT RESPIMAT (ipratropium bromide and albuterol) Inhalation Spray...

The Issue: Defective Delivery System: Inhalers do not spray properly, emitting either...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2015· JD & SN Inc., dba Moses Lake Professional Pharmacy

Recalled Item: TESTOSTERONE CYPIONATE FOR SUBQ INJECTION Recalled by JD & SN Inc., dba...

The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2015· JD & SN Inc., dba Moses Lake Professional Pharmacy

Recalled Item: TESTOSTERONE CYPIONATE (COMPOUNDED) Recalled by JD & SN Inc., dba Moses Lake...

The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2015· JD & SN Inc., dba Moses Lake Professional Pharmacy

Recalled Item: ALPROSTADIL/PROCAINE Recalled by JD & SN Inc., dba Moses Lake Professional...

The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2015· JD & SN Inc., dba Moses Lake Professional Pharmacy

Recalled Item: TESTOSTERONE PROPRIONATE Recalled by JD & SN Inc., dba Moses Lake...

The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry

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

Class II — Potential Health HazardOngoing
Refund