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 1626116280 of 29,186 recalls

Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Bio-Stable 5F DL-55CM IR-145 Kit Non-Valved with Nitinol GW PG Recalled by...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: RS 5F DL XPP KIT Recalled by Angiodynamics Inc. (Navilyst Medical Inc.) Due...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Bio-Stable 5F SL-55CM MST-70 Kit Valved with Nitinol Guidewire PG Recalled...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: CAN 5F DL BIOFLO PASV PICC NURSING TRAY Recalled by Angiodynamics Inc....

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: RS 5F DL BIOFLO PASV Recalled by Angiodynamics Inc. (Navilyst Medical Inc.)...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: RS 5F DL XCELA PICC Recalled by Angiodynamics Inc. (Navilyst Medical Inc.)...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Microintroducer Kit Recalled by Angiodynamics Inc. (Navilyst Medical Inc.)...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: RS 5F DL BIOFLO PASV Recalled by Angiodynamics Inc. (Navilyst Medical Inc.)...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: RS TANDEM 5F DL BIOFLO PICC Recalled by Angiodynamics Inc. (Navilyst Medical...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BioFlo PICC (Valved) 5FDL-55cm Maximal Barrier Nursing Kit PG Recalled by...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BioFlo PICC (NV) 5FDL-55cm Maximal Barrier Nursing Kit w/70cm Nitinol Wire...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved with Nitinol Guidewire PG...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: TANDEM 5F DL BIOFLO PASV Recalled by Angiodynamics Inc. (Navilyst Medical...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2018· Konica Minolta Medical Imaging USA, Inc.

Recalled Item: CS-7 Recalled by Konica Minolta Medical Imaging USA, Inc. Due to Panasonic...

The Issue: Panasonic has issued a Mandatory Product Safety Notice, indicating a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products PHYT Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: There is a potential for imprecise results when using the slides. Increase...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2018· Konica Minolta Medical Imaging USA, Inc.

Recalled Item: ImagePilot Recalled by Konica Minolta Medical Imaging USA, Inc. Due to...

The Issue: Panasonic has issued a Mandatory Product Safety Notice, indicating a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Stryker Sustainability Solutions

Recalled Item: Reprocessed HARMONIC Ace¿ +7 Recalled by Stryker Sustainability Solutions...

The Issue: Stryker Sustainability Solutions has received an increase in reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Zeiss, Carl Inc

Recalled Item: Cell Observer SD Recalled by Zeiss, Carl Inc Due to In certain eyepiece...

The Issue: In certain eyepiece configurations the laser shutter may not close...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Vyaire Medical

Recalled Item: AirLife Resuscitation Device Recalled by Vyaire Medical Due to An error in...

The Issue: An error in manufacturing of the AirLife Resuscitation Devices that has the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 8, 2018· Vyaire Medical

Recalled Item: AirLife Resuscitation Device Recalled by Vyaire Medical Due to An error in...

The Issue: An error in manufacturing of the AirLife Resuscitation Devices that has the...

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

Class I — Serious Health HazardOngoing