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. 2,271 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,271 in last 12 months

Showing 4654146560 of 48,326 recalls

FoodSeptember 18, 2012· Dale & Thomas Popcorn, LLC

Recalled Item: Popcorn Indiana Chocolate Peanut Butter Kettlecorn Net Wt 5 oz. Recalled by...

The Issue: Various flavors of popcorn were manufactured on a conveyor belt which tested...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 18, 2012· Dale & Thomas Popcorn, LLC

Recalled Item: Popcorn Indiana Drizzled Cinnamon Sugar Kettlecorn Net Wt. 5.5 oz. Recalled...

The Issue: Various flavors of popcorn were manufactured on a conveyor belt which tested...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 18, 2012· Iris Diagnostics

Recalled Item: Iris Diagnostics Division iQ Control/Focus Set Recalled by Iris Diagnostics...

The Issue: The firm initiated this recall because complaints from customers reported...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Trophy Sas

Recalled Item: CareStream Dental Kodak 2200 Intraoral X-ray system Product Usage: The...

The Issue: There have been approximately 2% of the x-ray generators manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Trophy Sas

Recalled Item: CareStream Dental CS 2100 X-ray system Product Usage: The expected Recalled...

The Issue: There have been approximately 2% of the x-ray generators manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Trophy Sas

Recalled Item: CareStream Dental Kodak 2100 Intraoral X-ray system Product Usage: The...

The Issue: There have been approximately 2% of the x-ray generators manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Trophy Sas

Recalled Item: CareStream Dental CS 2200 X-ray system Product Usage: The expected Recalled...

The Issue: There have been approximately 2% of the x-ray generators manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Instratek, Incorporated

Recalled Item: Endotrig Trigger Release Sterile Micro Hook Blade Product Usage: The...

The Issue: Instratek, Inc.has received multiple complaints of the 1052 Trigger Finger...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Mx8000 IDT Whole Body Computed Tomography X-ray system Distributed by...

The Issue: The low contrast pins in the Image Quality (IQ) phantom deteriorates over...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Elekta, Inc.

Recalled Item: MOSAIQ MOSAIQ is an image-enabled electronic medical record system (EMR)...

The Issue: A patient was seriously mistreated after a user made and saved an...

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

Class II — Potential Health HazardOngoing
DrugSeptember 17, 2012· DermaCare, Inc.

Recalled Item: UP & UP brand Recalled by DermaCare, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non-Sterile Products: Laboratory findings of high...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2012· DermaCare, Inc.

Recalled Item: UP & UP brand Recalled by DermaCare, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non-Sterile Products: Laboratory findings of high...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 17, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDLab¿ 1265 system blood gas analyzer Product Usage: RAPIDLab...

The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint¿¿ 405 system blood gas analyzer Product PUsage: These...

The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDLab¿ 1240 system blood gas analyzer Product Usage: RAPIDLab...

The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint¿ 500 system blood gas analyzer Product Usage: RAPIDPoint...

The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDLab¿ 1245 system blood gas analyzer Product Usage: RAPIDLab...

The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint¿ 400 system blood gas analyzer Product Usage: These...

The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDLab¿ 1260 system blood gas analyzer Product Usage: RAPIDLab...

The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2012· KCI USA, Inc.

Recalled Item: BariAir Therapy System The BariAir Therapy System is a risk Recalled by KCI...

The Issue: KCI has issued a medical device correction for the BariAir Therapy System...

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

Class II — Potential Health HazardOngoing