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. 2,576 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,576 in last 12 months

Showing 1672116740 of 29,186 recalls

Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK BMG Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK C-Peptide II Recalled by Tosoh Bioscience Inc Due to Asfotase...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: Tosoh ST AIA-PACK HbA1c Pretreatment Solution Recalled by Tosoh Bioscience...

The Issue: The assay can potentially generate erroneously elevated or erroneously...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK HCG Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK Myoglobin Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK SHBG Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-PACK TSH 3rd Generation Recalled by Tosoh Bioscience Inc Due to Asfotase...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK IRI Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: Tosoh ST AIA-PACK HbA1c Calibrator Recalled by Tosoh Bioscience Inc Due to...

The Issue: The assay can potentially generate erroneously elevated or erroneously...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Synthes, Inc.

Recalled Item: Flex Arm Product Usage: The Synthes Flex Arm is a Recalled by Synthes, Inc....

The Issue: Quick connect feature of instruments may be unable to connect to the male...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 Ultrasound System. The firm name on the label Recalled by...

The Issue: The ECG signal may flatline due to electromagnetic interference during the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK FSH Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK Fer Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2018· Getinge Disinfection Ab

Recalled Item: Getinge AGS Recalled by Getinge Disinfection Ab Due to There is potential...

The Issue: There is potential for a cart with disinfected goods to unload without the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2018· Beckman Coulter Inc.

Recalled Item: BECKMAN COULTER iChemVELOCITY Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter has determined that there is a potential for incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2018· Getinge Disinfection Ab

Recalled Item: Getinge AGS Recalled by Getinge Disinfection Ab Due to There is potential...

The Issue: There is potential for a cart with disinfected goods to unload without the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2018· Randox Laboratories Ltd.

Recalled Item: Lipase Recalled by Randox Laboratories Ltd. Due to Randox has now released...

The Issue: Randox has now released further steps to avoid contamination of the Lipase...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius MRI Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer M/L Taper Hip Prosthesis Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Certain packages labeled as size 7.5 Extended Offset Reduced Neck length hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer M/L Taper Hip Prosthesis Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Certain packages labeled as size 7.5 Extended Offset Reduced Neck length hip...

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

Class II — Potential Health HazardOngoing