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. 2,400 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,400 in last 12 months

Showing 2230122320 of 48,326 recalls

Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Prime SP Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Prime Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Lightning Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Precision Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion One Vision Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Premium Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion One Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Hamilton Medical AG

Recalled Item: HAMILTON-G5 Recalled by Hamilton Medical AG Due to New software version for...

The Issue: New software version for affected ventilators reduces the probability of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2019· Change Healthcare Israel Ltd.

Recalled Item: McKesson Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...

The Issue: users are not notified of procedure medication discrepancies between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Change Healthcare Israel Ltd.

Recalled Item: Horizon Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...

The Issue: users are not notified of procedure medication discrepancies between the...

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

Class II — Potential Health HazardOngoing
DrugMarch 22, 2019· InvaGen Pharmaceuticals, Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by InvaGen Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2019· InvaGen Pharmaceuticals, Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by InvaGen Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2019· InvaGen Pharmaceuticals, Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by InvaGen Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2019· Auro Pharmacies Inc. DBA Central Drugs

Recalled Item: Biotin 10 mg/mL Injection Recalled by Auro Pharmacies Inc. DBA Central Drugs...

The Issue: Failed pH Specification: product does not meet pH label claim.

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

Class III — Low RiskOngoing
Refund
DrugMarch 22, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Fayosim (levonorgestrel and ethinyl estradiol) tablets USP Recalled by Lupin...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 22, 2019· Stryker Communications

Recalled Item: Berchtold Chromophare F628 Surgical Lights. Product Usage: The medical...

The Issue: The back cover of the light head was insufficiently assembled and could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Stryker Communications

Recalled Item: Berchtold Chromophare F528 Surgical Lights. Product Usage: The medical...

The Issue: The back cover of the light head was insufficiently assembled and could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Cardinal Health 200, LLC

Recalled Item: ChemoPlus Chemo Spill Kit Product Code:CT4004 Product Usage: ChemoPlus...

The Issue: Kit label states not made with natural rubber latex,however safety goggles...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Cios Alpha with software version VA30-mobile C-arm x-ray Material # Recalled...

The Issue: Continuous operation of the Cios Alpha at high tube outputs may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Cardinal Health 200, LLC

Recalled Item: ChemoPlus Chemo Spill Kit Recalled by Cardinal Health 200, LLC Due to Kit...

The Issue: Kit label states not made with natural rubber latex,however safety goggles...

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

Class II — Potential Health HazardOngoing