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 4044140460 of 48,326 recalls

Medical DeviceAugust 8, 2014· Bard Access Systems

Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...

The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· Bard Access Systems

Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...

The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· Bard Access Systems

Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...

The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· Bard Access Systems

Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...

The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· Bard Access Systems

Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...

The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...

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

Class II — Potential Health HazardOngoing
DrugAugust 8, 2014· Cubist Pharmaceuticals, Inc.

Recalled Item: CUBICIN (daptomycin for injection) 500 mg Recalled by Cubist...

The Issue: Presence of Particulate Matter: Foreign particulate matter (tiny black...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 7, 2014· Baxter Healthcare Corp.

Recalled Item: Dianeal Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 2.5%...

The Issue: Presence of Particulate Matter: particulate matter was found during the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 7, 2014· Zimmer, Inc.

Recalled Item: PERSONA The Personalized Knee System Constrained Tibial Articular Surface...

The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2014· Zimmer, Inc.

Recalled Item: PERSONA The Personalized Knee System PS Tibial Articular Surface Provisional...

The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2014· Zimmer, Inc.

Recalled Item: PERSONA The Personalized Knee System Constrained Posterior Stabilized Tibial...

The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2014· Zimmer, Inc.

Recalled Item: PERSONA" The Personalized Knee System UC Tibial Articular Surface...

The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2014· Zimmer, Inc.

Recalled Item: PERSONA The Personalized Knee System Tibial Articular Surface Provisional...

The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2014· Zimmer, Inc.

Recalled Item: PERSONA The Personalized Knee System CR Tibial Articular Surface Provisional...

The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Sedecal S.A.

Recalled Item: MobileDiagnost wDR motorized portable diagnostic X-ray systems. Recalled by...

The Issue: Reports of unexpected movement.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Siemens Healthcare Diagnostics

Recalled Item: ADVIA Chemistry A1c_3 CAL (Calibrator) for use on the ADVIA Chemistry...

The Issue: The ADVIA Chemistry Systems A1c_3 method may exhibit a percent bias of -9%...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Angiodynamics, Inc.

Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....

The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Arrow International Inc

Recalled Item: Arrow Select Kits (ASK) and Maximal Barrier Precautions Kits (CDC) Recalled...

The Issue: The component supplier recalled their 0.9% Sodium Chloride Injection USP BD...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Ellex iScience, Inc.

Recalled Item: iTRACK250A Canaloplasty Microcatheter Kit Recalled by Ellex iScience, Inc....

The Issue: One lot may not have been properly sealed, resulting in a non-sterile device.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Angiodynamics, Inc.

Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....

The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2014· Parker Laboratories, Inc.

Recalled Item: Parker Eclipse Probe Cover Recalled by Parker Laboratories, Inc. Due to...

The Issue: Parker Laboratories, Inc. received a report of an incorrect expiration date...

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

Class II — Potential Health HazardOngoing