Product Recalls in Montana

Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,876 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
1,876 in last 12 months

Showing 1578115800 of 27,852 recalls

Medical DeviceMay 10, 2018· Anika Therapeutics, Inc.

Recalled Item: Hyalomatrix Recalled by Anika Therapeutics, Inc. Due to Hyalomatrix products...

The Issue: Hyalomatrix products are susceptible to degradation as a result of the...

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) 5FSL-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 IR-145 Kit Non-Valved PG Recalled by Angiodynamics...

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: 5F DL BIOFLO PICC 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: RS TANDEM 5F DL XPP 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: BioFlo Midline 5F DL-20cm MST-45 Kit w/ Two Nitinol Guidewires 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: 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: 5F DL BIOFLO PASV 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: CAN 5F SINGLE XCELA 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: RS - TANDEM 5F DL BIOFLO MIDLINE Recalled by Angiodynamics Inc. (Navilyst...

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

Recalled Item: Bio-Stable 5F SL-55CM IR-145 Kit Valved PG 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· Zimmer Dental Inc

Recalled Item: Outer Package Label: Tapered Screw-Vent Implant System Recalled by Zimmer...

The Issue: Dental implants have incorrect item/lot numbers and size on the inner...

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 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 10, 2018· FHC, Inc.

Recalled Item: microTargeting" STar" Drive System (Motorized) Recalled by FHC, Inc. Due to...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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 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: 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 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Drive System Distributed by Medtronic Recalled by FHC, Inc....

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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