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. 2,387 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,387 in last 12 months

Showing 2348123500 of 48,326 recalls

DrugSeptember 19, 2018· Upsher Smith Laboratories, Inc.

Recalled Item: Bumetanide Tablets Recalled by Upsher Smith Laboratories, Inc. Due to Failed...

The Issue: Failed impurities/ degradation specifications: Product is Out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 19, 2018· Pfizer Inc.

Recalled Item: Elelyso (taliglucerase alfa) for injection Recalled by Pfizer Inc. Due to...

The Issue: Lack of assurance of sterility -Reports of loose metal ferrule crimps on...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 19, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: Philips DigitalDiagnost software 4.1.x and 4.2.x Recalled by Philips Medical...

The Issue: Stitching run on SkyPlate detector interrupted intermittently; Stitching...

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

Class II — Potential Health HazardOngoing
DrugSeptember 18, 2018· Xiromed LLC

Recalled Item: Altavera Levonorgestrel and Ethinyl Estradiol Tablets Recalled by Xiromed...

The Issue: Labeling: Not Elsewhere Classified: mislabeling of the Altavera generic name...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 18, 2018· Beckman Coulter Inc.

Recalled Item: The Access Cortisol Reagent. REF (Catalog Number) 33600 Recalled by Beckman...

The Issue: Cross contamination may have occurred between wells for the reagent pack. As...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2018· COVIDIEN LLC

Recalled Item: Puritan Bennett 980 (PB980) ventilator series: Puritan Bennett" 980...

The Issue: Software Update: External USB Drive performance and its impact on Graphic...

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

Class I — Serious Health HazardOngoing
DrugSeptember 17, 2018· Medline Industries Inc

Recalled Item: SparkleFresh Fluoride Toothpaste Recalled by Medline Industries Inc Due to...

The Issue: Microbial Contamination of Non-Sterile Product

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2018· Endo Pharmaceuticals, Inc.

Recalled Item: robaxin-750 (methocarbamol tablets Recalled by Endo Pharmaceuticals, Inc....

The Issue: Labeling: Incorrect Instructions: Dosage information on the immediate...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 17, 2018· Otsuka Pharmaceutical Development & Commercialization, Inc.

Recalled Item: treatNOW ABILIFY (aripiprazole) / ABILIFY MAINTENA 400-mg (aripiprazole) for...

The Issue: Labeling Not Elsewhere Classified: Physician sample kits/cartons of treatNOW...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 17, 2018· Otsuka Pharmaceutical Development & Commercialization, Inc.

Recalled Item: treatNOW ABILIFY (aripiprazole) and ABILIFY MAINTENA (aripiprazole) 400MG...

The Issue: Labeling Not Elsewhere Classified: Physician sample kits/cartons of treatNOW...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 17, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: Medtronic Navigation 0-arm 02 Imaging System interventional fluoroscopic...

The Issue: O-arm 02 Imaging Systems correction to software version 4.1.0; new version...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2018· Leica Microsystems, Inc.

Recalled Item: BOND Slide Labeler Zebra Printer Model TLP3842 and Model GX4301 Recalled by...

The Issue: The power supply unit for the printer used with the device can potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2018· BioMerieux SA

Recalled Item: NucliSENS¿ Magnetic Extraction Reagents Recalled by BioMerieux SA Due to...

The Issue: Data loggers showed that one shipment to the United States experienced low...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2018· Sterilmed, Inc.

Recalled Item: Reprocessed Agilis Steerable Introducer: indicated for introducing various...

The Issue: Reprocessed Agilis Steerable Introducers may not meet endotoxin requirements...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· GE Healthcare, LLC

Recalled Item: GE LOGIQ E10 Ultrasound System Recalled by GE Healthcare, LLC Due to There...

The Issue: There is a potential for an undetected over temperature condition on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· GE Healthcare, LLC

Recalled Item: GE Healthcare Millennium MC Recalled by GE Healthcare, LLC Due to A detector...

The Issue: A detector can detach and fall.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 14, 2018· GE Healthcare, LLC

Recalled Item: GE Healthcare Millennium MG Multi-Geometry Digital CSE Dual Detector Gamma...

The Issue: A detector can detach and fall.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 14, 2018· Luminex Corporation

Recalled Item: VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as...

The Issue: Potential to lead to a false negative results.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· GE Healthcare, LLC

Recalled Item: GE Healthcare Millennium MyoSIGHT Nuclear Cardiology Imaging System H3000ZH...

The Issue: A detector can detach and fall.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 14, 2018· Ecolab Inc

Recalled Item: Instrument Arm Drape (Box of 20) individually sealed in poly-Tyvek Recalled...

The Issue: The pouches of certain lots of product may have wrinkles along the pouch...

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

Class II — Potential Health HazardOngoing