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 4040140420 of 48,326 recalls

Medical DeviceAugust 15, 2014· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Howmedica Osteonics RESTORATION Acetabular Augment System Recalled...

The Issue: The peel strength of the inner blister may have been below internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2014· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Triathlon femoral component. Howmedica Osteonics Corp....

The Issue: The peel strength of the inner blister may have been below internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2014· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Scorpio femoral component. Howmedica Osteonics Corp....

The Issue: The peel strength of the inner blister may have been below internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2014· Lumenis, Inc.

Recalled Item: Array LaserLink Recalled by Lumenis, Inc. Due to Lumenis initiated a...

The Issue: Lumenis initiated a field-correction for the Array Laser Link",...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2014· Data Innovations, LLC

Recalled Item: ProVue Instrument Driver for JResultNet (ProVue.jrm) v. 1.5.3 and below...

The Issue: Potential issues with the ProVue driver have been identified which may cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2014· The Anspach Effort, Inc.

Recalled Item: Synthes Small Electric Drive (SED). For use in general traumatology....

The Issue: The affected Small Electric Drive (SED) may operate solely in reverse mode,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2014· Sam Medical Products

Recalled Item: SAM Junctional Tourniquet (SJT) Auxiliary Recalled by Sam Medical Products...

The Issue: SAM Junctional Tourniquet (SJT) Auxiliary strap, model SJT 102 and SJT 112,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ HbA1c Recalled by Siemens Healthcare Diagnostics, Inc. Due...

The Issue: In March, Siemens Healthcare Diagnostics issued an Urgent Medical Device...

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

Class II — Potential Health HazardOngoing
DrugAugust 13, 2014· VistaPharm, Inc.

Recalled Item: METOCLOPRAMIDE ORAL SOLUTION Recalled by VistaPharm, Inc. Due to Defective...

The Issue: Defective Container: Product leaks when inverted.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2014· Fresenius Kabi USA, LLC

Recalled Item: PROPRANOLOL HYDROCHLORIDE INJECTION Recalled by Fresenius Kabi USA, LLC Due...

The Issue: CGMP Deviations: Citations given to API supplier by the Italian Health...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 13, 2014· Maquet Cardiovascular, LLC

Recalled Item: Acrobat V Vacuum Off-Pump System OM-9100S Acrobat SUV Vacuum Off-Pump...

The Issue: An internal finding identified the presence of pinholes/cuts in some of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Biofire Defense

Recalled Item: JBAIDS Instrument System Software version 3.5.0.72. The JBAIDS instrument is...

The Issue: BioFire Defense, LLC is initiating a field action for JBAIDS Software...

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Water may leak...

The Issue: Water may leak into the center gas lumen of the Patient Circuit

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Smith & Nephew, Inc.

Recalled Item: RENASYS EZ Negative Pressure Wound Therapy (NPWT) System (RENASYS EZ)...

The Issue: Modification were made to the RENASYS EZ NPWT Systems without a 510(k) or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing