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. 2,371 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,371 in last 12 months

Showing 2594125960 of 48,326 recalls

Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

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

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
DrugMarch 5, 2018· Johnson Matthey Inc.

Recalled Item: Morphine Sulfate USP Milled Recalled by Johnson Matthey Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: Bioburden out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2018· InvaGen Pharmaceuticals, Inc.

Recalled Item: Decitabine for Injection Recalled by InvaGen Pharmaceuticals, Inc. Due to...

The Issue: Failed impurities/degradation specifications: Failure to water content and...

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

Class III — Low RiskOngoing
Refund
DrugMarch 5, 2018· Sagent Pharmaceuticals Inc

Recalled Item: methylPREDNISolone Sodium Succinate for Injection Recalled by Sagent...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2018· Sagent Pharmaceuticals Inc

Recalled Item: methylPREDNISolone Sodium Succinate for Injection Recalled by Sagent...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2018· Sagent Pharmaceuticals Inc

Recalled Item: methylPREDNISolone Sodium Succinate for Injection Recalled by Sagent...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2018· Novel Laboratories, Inc.

Recalled Item: Lupin Hydrocodone Bitartrate and Homatropine Methylbromide Tablets Recalled...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugMarch 2, 2018· Renaissance Lakewood, LLC

Recalled Item: Flucanazole Injection Recalled by Renaissance Lakewood, LLC Due to...

The Issue: Superpotent and Failed Stability Specifications; out of specification...

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

Class III — Low RiskOngoing
Refund
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 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· 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 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius Tiro M 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· 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· Draeger Medical, Inc.

Recalled Item: Fabius GS Premium 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· Draeger Medical, Inc.

Recalled Item: Fabius Tiro 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· bioMerieux, Inc.

Recalled Item: VIDAS LH Recalled by bioMerieux, Inc. Due to Several complaints were...

The Issue: Several complaints were received for invalid calibration with low calibrator...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Biomet, Inc.

Recalled Item: Zimmer Biomet Comprehensive Segmental Revision System (SRS). Orthopedic...

The Issue: During assembly, an SRS Humeral Distal Body implant failed to engage...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: Neonatal PICC Tray Recalled by Vygon U.S.A. Due to Potential friction holes...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: Maximum Barrier Tray Recalled by Vygon U.S.A. Due to Potential friction...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing