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. 2,334 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,334 in last 12 months

Showing 3690136920 of 48,326 recalls

Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Stripper Recalled by American Medical Systems Innovation Center - Silicon...

The Issue: validation data related to cleaning instructions and sterilization methods...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2015· Integra LifeSciences Corp.

Recalled Item: Integra Camino Intracranial Pressure Monitoring Catheter with Licox IMC Bolt...

The Issue: Integra LifeSciences is recalling the Camino Intracranial Pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2015· Bard Access Systems

Recalled Item: PowerPICC SOLO Catheter with Sherlock 3CG TPS Stylet 4F Maximal Recalled by...

The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...

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

Class III — Low RiskOngoing
Medical DeviceMay 27, 2015· Bard Access Systems

Recalled Item: PowerPICC SOLO2 Catheter 4F Maximal Barrier Tray with Microintroducer...

The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...

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

Class III — Low RiskOngoing
Medical DeviceMay 27, 2015· Bard Access Systems

Recalled Item: PowerPICC SOLO Catheter with Sherlock 3CG (TPS) Stylet 5F Maximal Recalled...

The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...

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

Class III — Low RiskOngoing
Medical DeviceMay 27, 2015· Bard Access Systems

Recalled Item: PowerPICC SOLO Catheter with Tip Location System (TLS) Stylet 4F Recalled by...

The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...

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

Class III — Low RiskOngoing
Medical DeviceMay 27, 2015· Musculoskeletal Transplant Foundation, Inc.

Recalled Item: Allofix Insertion Kit Recalled by Musculoskeletal Transplant Foundation,...

The Issue: Musculoskeletal Transplant Foundation is recalling a certain lot of Allofix...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2015· Synthes, Inc.

Recalled Item: DePuy Synthes 6.5 mm Titanium Recon Screws w/T25 Stardrive (70mm Recalled by...

The Issue: certain lots of the Titanium Recon Screws (6.5mm ) were found to contain the...

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

Class II — Potential Health HazardOngoing
FoodMay 27, 2015· Novacare, LLC

Recalled Item: Glucosamine 750 mg 120 ct Recalled by Novacare, LLC Due to TSN Labs is...

The Issue: TSN Labs is conducting a field action on Glucosamine 750 mg 120 ct due to...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugMay 27, 2015· Bracco Diagnostic Inc

Recalled Item: E-Z-CAT Dry Barium Sulfate for Suspension (2% w/w after mixing) Recalled by...

The Issue: Failed stability specifications:This recall has been initiated due to out of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 26, 2015· Bausch & Lomb Surgical, Inc.

Recalled Item: Bausch & Lomb SofPort Advanced Optics Aspheric Lens Recalled by Bausch &...

The Issue: Haptics breaking during lens loading and insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2015· Smiths Medical ASD, Inc.

Recalled Item: CADD¿- Solis Ambulatory Infusion Pump Recalled by Smiths Medical ASD, Inc....

The Issue: Smiths Medical has become aware of an issue with an intermittent occurrence...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2015· Bausch & Lomb Surgical, Inc.

Recalled Item: Bausch & Lomb SoFlex SE Foldable intraocular Lens Product Usage: Recalled by...

The Issue: Haptics breaking during lens loading and insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/ zeego systems Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: There exists a possible position sensor fault in the swivel base axis not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 0702-001-350Q Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Stryker Instruments is initiating a recall of the Neptune 2 Waste Management...

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

Class II — Potential Health HazardOngoing
DrugMay 22, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Divalproex Sodium Extended-Release Tablets Recalled by Dr. Reddy's...

The Issue: Failed Dissolution Specifications; exceeded specification at the 9 hour time...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Divalproex Sodium Extended-Release Tablets Recalled by Dr. Reddy's...

The Issue: Failed Dissolution Specifications; exceeded specification at the 9 hour time...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 22, 2015· Vitamin Cottage Natural Food Markets, Inc.

Recalled Item: Natural Grocers Raw Macadamia Nuts Recalled by Vitamin Cottage Natural Food...

The Issue: Vitamin Cottage Natural Food Markets Inc. is recalling various lots of...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 21, 2015· Elekta, Inc.

Recalled Item: Oncentra Brachy radiation therapy planning software designed to analyze and...

The Issue: Incorrect dose calculation for Regions of Interest (ROIs) defined on a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2015· Exactech, Inc.

Recalled Item: Exactech Ambassador Cervical Plate System The Exactech Ambassador Cervical...

The Issue: Shipped to a single consignee prior to completion of final inspection.

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

Class II — Potential Health HazardOngoing