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. 2,518 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,518 in last 12 months

Showing 2062120640 of 29,186 recalls

Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core128 Model No. 728323 Recalled by Philips Medical Systems...

The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT SP Model No. 728311 Recalled by Philips Medical Systems...

The Issue: Software issues found in v4.1 .3/4.1.5 in the Philips Brilliance iCT/ iCT SP...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 CT Model 728231 Recalled by Philips Medical Systems...

The Issue: Software issues found in software versions v4.1.3/4.1.4/4.1.5 in the Philips...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Model No. 728321 Recalled by Philips Medical Systems...

The Issue: Software issues in software versions v4.1.3/4.1.4/4.1.5 in the Philips...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: Software issues in versions v4.1 .3/4.1.5 in the Philips Brilliance iCT) iCT...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT Model No. 728326 Recalled by Philips Medical Systems...

The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2016· Excelsior Medical Corp

Recalled Item: Excelsior Disposable Syringe Heparin Lock Flush Recalled by Excelsior...

The Issue: Certain lots of Heparin Lock Flush, USP Syringes (5 ml Fill in 10 ml...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2016· CMP Industries, Llc

Recalled Item: IMPAK ELASTIC ACRYLIC RESIN POWDER & LIQUID Recalled by CMP Industries, Llc...

The Issue: Possible presence of foreign material (rust).

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2016· CMP Industries, Llc

Recalled Item: IMPAK Liquid Acrylic Resin sold under the following labels: 1) Recalled by...

The Issue: Possible presence of foreign material (rust).

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur XPT Immunoassay System Recalled by Siemens Healthcare...

The Issue: The ADVIA Centaur¿ XPT default setting for the Daily Maintenance Task (Daily...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2016· STERILMED, INC.

Recalled Item: Reprocessed Microline Scissor Tips intended to be used with a Recalled by...

The Issue: Sterlilmed is recalling all unexpired Scissor Tips because of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2016· Greiner Bio-One North America, Inc.

Recalled Item: 4 ml FX Sodium Fluoride/Potassium Oxalate tube Recalled by Greiner Bio-One...

The Issue: The 4 ml FX Sodium Fluoride/Potassium Oxalate tube may have no or low...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Toshiba American Medical Systems Inc

Recalled Item: Toshiba America Medical Systems Recalled by Toshiba American Medical Systems...

The Issue: It has been found that if the scan range extends beyond the maximum Field of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT-S(64) 4R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: The bracket that is used to lift the cover has bolts that were not welded in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT S(20) - 3R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: The bracket that is used to lift the cover has bolts that were not welded in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Volcano Corporation

Recalled Item: Volcano s5 Recalled by Volcano Corporation Due to Volcano has become aware...

The Issue: Volcano has become aware of an incompatibility issue between Impacted...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Toshiba American Medical Systems Inc

Recalled Item: Toshiba America Medical Systems Recalled by Toshiba American Medical Systems...

The Issue: It has been found that if the scan range extends beyond the maximum Field of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· GSK Consumer Healthcare

Recalled Item: Breathe Right Clear Recalled by GSK Consumer Healthcare Due to Some cartons...

The Issue: Some cartons used in the secondary packaging of Breathe Right Clear, Large,...

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

Class III — Low RiskOngoing
Medical DeviceApril 25, 2016· Toshiba American Medical Systems Inc

Recalled Item: Toshiba America Medical Systems Recalled by Toshiba American Medical Systems...

The Issue: It has been found that if the scan range extends beyond the maximum Field of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Toshiba American Medical Systems Inc

Recalled Item: Toshiba America Medical Systems Recalled by Toshiba American Medical Systems...

The Issue: It has been found that if the scan range extends beyond the maximum Field of...

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

Class II — Potential Health HazardOngoing