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. 2,470 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,470 in last 12 months

Showing 1576115780 of 48,326 recalls

Medical DeviceFebruary 18, 2021· TELEFLEX MEDICAL INC

Recalled Item: RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct...

The Issue: Teleflex is voluntarily recalling the products above due to customers...

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

Class II — Potential Health HazardOngoing
DrugFebruary 17, 2021· Edge Pharma, LLC

Recalled Item: Methacholine Challenge 5-Syringe Test Kits Recalled by Edge Pharma, LLC Due...

The Issue: Temperature Abuse; labeled with the incorrect room temperature (15-25 ¿C)...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 17, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Imatinib Mesylate Tablets 100mg Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 16, 2021· Vectornate USA Inc

Recalled Item: MedSchenker Smart Transport Medium (STM) System: CULTURE MEDIA Recalled by...

The Issue: Discoloration and turbidity were present in the specified lots of STMs...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2021· Clerio Vision

Recalled Item: EXTREME H2O 59% (hioxifilcon A) spherical soft contact lens for Recalled by...

The Issue: Contact lenses may be mislabeled with the incorrect lens power.

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

Class II — Potential Health HazardOngoing
DrugFebruary 15, 2021· Adams.Secret.co

Recalled Item: Adam's Secret Extra Strength 1500 Recalled by Adams.Secret.co Due to...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 15, 2021· Adams.Secret.co

Recalled Item: Adam's Secret Extra Strength 3000 Recalled by Adams.Secret.co Due to...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 15, 2021· Teva Pharmaceuticals USA

Recalled Item: Metoclopramide Injection USP Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Chemical contamination; Unknown brown residue adhering to the inside of one...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 15, 2021· CARESTREAM DENTAL, LLC

Recalled Item: Carestream Dental CS 3600 Single Use Normal Tips Recalled by CARESTREAM...

The Issue: The mirror may become detached and fall from the unit

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Nuvasive Specialized Orthopedics Inc

Recalled Item: NUVASIVE PRECICE UNYTE System (Humerus and Tibia): PRECICE Trauma Nail...

The Issue: Due to not having the full complement of biological assessments for all...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Nuvasive Specialized Orthopedics Inc

Recalled Item: NUVASIVE FREEDOM: End Cap for PRECICE Intramedullary Limb Lengthening System...

The Issue: Due to not having the full complement of biological assessments for all...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Nuvasive Specialized Orthopedics Inc

Recalled Item: NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System...

The Issue: Due to not having the full complement of biological assessments for all...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Nuvasive Specialized Orthopedics Inc

Recalled Item: PRECICE PLATE - Product Usage: intended for limb lengthening Recalled by...

The Issue: Due to complaints of adverse events potentially related to biological...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Nuvasive Specialized Orthopedics Inc

Recalled Item: PRECICE STRYDE - Product Usage: intended for limb lengthening Recalled by...

The Issue: Due to complaints of adverse events potentially related to biological...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Nuvasive Specialized Orthopedics Inc

Recalled Item: Precice Bone Transport - Product Usage: intended for limb lengthening...

The Issue: Due to complaints of adverse events potentially related to biological...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· TELEFLEX MEDICAL INC

Recalled Item: PLEUR-EVAC Thoracic Catheters (CATHETER Recalled by TELEFLEX MEDICAL INC Due...

The Issue: Teleflex is recalling this product due to a lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS SARS-CoV-2 Antigen Reagent Pack - The VITROS Immunodiagnostic...

The Issue: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen False Reactive Results...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Reagent- In Vitro...

The Issue: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen False Reactive Results...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Medtronic Vascular, Inc.

Recalled Item: Valiant Navion Thoracic Stent Graft System. For endovascular repair of...

The Issue: Due to the presence of type IIIb endoleaks, stent fractures, and stent ring...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 11, 2021· Hollister Incorporated

Recalled Item: Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and...

The Issue: The tube holder can separate from the barrier that secures the device to the...

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

Class II — Potential Health HazardOngoing