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. 2,306 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,306 in last 12 months

Showing 4276142780 of 48,326 recalls

Medical DeviceOctober 17, 2013· Baxter Healthcare Corp

Recalled Item: 15 L Cycler Drainage Bag Product Usage: For use with Recalled by Baxter...

The Issue: The large tube clamp used to close the drain tube on the 15 L Cycler...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Na+ Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics has recalled VITROS Chemistry Products Na+ Slides...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Calibrator Kit 2 Recalled by Ortho-Clinical...

The Issue: Ortho Clinical Diagnostics has recalled VITROS Chemistry Products Na+ Slides...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Zimmer, Inc.

Recalled Item: Trabecular Metal" Reverse Shoulder System Recalled by Zimmer, Inc. Due to As...

The Issue: As a result of complaints for disassociation of the TM Reverse Glenosphere...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Philips Medical Systems North America Inc.

Recalled Item: EPIQ 7 Ultrasound System Recalled by Philips Medical Systems North America...

The Issue: A problem has been detected with Philips Model EPIQ 7 Ultrasound System,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Spacelabs Healthcare, Llc

Recalled Item: Spacelabs Healthcare qube Compact Patient Monitor Recalled by Spacelabs...

The Issue: Spacelabs Healthcare qube Compact Patient Monitor, Model 91390, may fail to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Del Mar Reynolds Medical, Ltd.

Recalled Item: CAS I/II Absorbers that are parts of the BleaseSirius Anesthesia Workstation...

The Issue: Spacelabs Healthcare Ltd. of United Kingdom recalls , and Service Kits, Part...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 17, 2013· GlaxoSmithKline, LLC.

Recalled Item: Biotene Moisturizing Mouth Spray Recalled by GlaxoSmithKline, LLC. Due to...

The Issue: Label indicates, "Sweetened with xylitol and Sorbitol", however product does...

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

Class II — Potential Health HazardOngoing
DrugOctober 16, 2013· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Ciclopirox Shampoo 1% Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...

The Issue: Subpotent. drug

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 16, 2013· Baxter Healthcare Corp.

Recalled Item: The HomeChoice Pro APD System is a peritoneal dialysis system. Recalled by...

The Issue: The occluder in affected devices 1) may have sharp edges that could cut the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2013· Bausch & Lomb Surgical, Inc.

Recalled Item: Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos Recalled by Bausch &...

The Issue: Lens was manufactured with incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2013· Microgenics Corp

Recalled Item: Thermo Fisher Scientific/Microgenics brand CEDIA Tobramycin II Assay...

The Issue: Microgenics Corp., part of Thermo Fisher Scientific, is recalling CEDIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2013· Cutera, Inc.

Recalled Item: Cutera brand truSculpt infrared System (optional) Recalled by Cutera, Inc....

The Issue: Cutera received two adverse events associated with the edge of the...

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

Class II — Potential Health HazardOngoing
DrugOctober 15, 2013· B. Braun Medical Inc

Recalled Item: Cefepime for Injection USP and Dextrose Injection USP Recalled by B. Braun...

The Issue: Presence of Particulate Matter: The 1g Cefepime for Injection USP and...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 15, 2013· VistaPharm, Inc.

Recalled Item: Phenytoin Oral Suspension USP 125mg/5mL Recalled by VistaPharm, Inc. Due to...

The Issue: Defective Container: A lidding deformity allowed for the product to have out...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 15, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Material Mix (Adjustable Cervical Distractor-Right Recalled by...

The Issue: One material batch used for production of the affected parts of the Synthes...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2013· Teleflex Medical

Recalled Item: Green Rusch - Lite Disposable Metal Laryngoscope Ridge Blade to Recalled by...

The Issue: Labeling inconsistency

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Philips Medical Systems, Inc.

Recalled Item: Philips Multi Diagnost Eleva II Recalled by Philips Medical Systems, Inc....

The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Philips Medical Systems, Inc.

Recalled Item: Philips Multi Diagnost Eleva with FlatDetector Recalled by Philips Medical...

The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Synthes (USA) Products LLC

Recalled Item: Synthes 14.5 mm Outer Protection Sleeve for Suprapatellar Synthes 14.5...

The Issue: Complaints were received reporting that a product packaged as a 14.5 mm...

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

Class II — Potential Health HazardOngoing