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. 2,322 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,322 in last 12 months

Showing 4126141280 of 48,326 recalls

Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· DeVilbiss Healthcare LLC

Recalled Item: DeVilbiss Model DV5x Series CPAP units. For use in treating Recalled by...

The Issue: A limited number of DV5x Series CPAP units were manufactured and shipped...

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

Class III — Low RiskOngoing
Medical DeviceMay 13, 2014· CooperSurgical, Inc.

Recalled Item: Cooper Surgical TAMPA CATHETER 5 French 33 cm. Intended for Recalled by...

The Issue: Sterility of the device may be compromised due to unsealed pouch

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: The NAV3i Platform Power Box supplies the electrical components with...

The Issue: The Stryker NAV3i Platform Power Boxes produced between December 9, 2013 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: The Stryker NAV3i Platform is a mobile cart platform consisting Recalled by...

The Issue: The Stryker NAV3i Platform Power Boxes produced between December 9, 2013 and...

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

Class II — Potential Health HazardOngoing
DrugMay 12, 2014· Bristol-Meyers Squibb

Recalled Item: COUMADIN FOR INJECTION (Warfarin Sodium for Injection Recalled by...

The Issue: Presence of Particulate Matter: particulate matter identified as...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 12, 2014· Baxter Healthcare Corp.

Recalled Item: 0.9 % Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...

The Issue: Presence of Particulate Matter; blue polyisoprene shavings found inside the...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 12, 2014· John W Hollis Inc

Recalled Item: Polidocanol 1% Solution for Injection Recalled by John W Hollis Inc Due to...

The Issue: Lack of Assurance of Sterility: Lack of sterility assurance in compounded...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 12, 2014· John W Hollis Inc

Recalled Item: Polidocanol 0.5% Solution for Injection Recalled by John W Hollis Inc Due to...

The Issue: Lack of Assurance of Sterility: Lack of sterility assurance in compounded...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 12, 2014· John W Hollis Inc

Recalled Item: Mannitol 5% Solution for injection Recalled by John W Hollis Inc Due to Lack...

The Issue: Lack of Assurance of Sterility: Lack of sterility assurance in compounded...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 12, 2014· John W Hollis Inc

Recalled Item: Papaverine HCl 30 mg Recalled by John W Hollis Inc Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Lack of sterility assurance in compounded...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 12, 2014· John W Hollis Inc

Recalled Item: Papaverine HCl 30 mg Recalled by John W Hollis Inc Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Lack of sterility assurance in compounded...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 12, 2014· John W Hollis Inc

Recalled Item: Levocarnitine Solution for injection Recalled by John W Hollis Inc Due to...

The Issue: Lack of Assurance of Sterility: Lack of sterility assurance in compounded...

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

Class II — Potential Health HazardOngoing
Refund