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 4094140960 of 48,326 recalls

Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Connection QRG for the da Vinci Standard Surgical System Recalled by...

The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Stapler Addendum for the da Vinci Standard Surgical System Recalled by...

The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Insert for IRK for the da Vinci Standard Surgical System Recalled by...

The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Vision Troubleshooting Guide for the da Vinci Standard Surgical System...

The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Cautery QRG for the da Vinci Standard Surgical System Recalled by Intuitive...

The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Vessel Sealer QRG for the da Vinci Standard Surgical System Recalled by...

The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Single Site US Manuals and Single Site OUS Manuals for Recalled by Intuitive...

The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Natural Rubber Latex QRG for the da Vinci Standard Surgical System Recalled...

The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Vessel Sealer Addendum for the da Vinci Standard Surgical System Recalled by...

The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Endowrist Instrument and Accessory Manual for the da Vinci Standard Recalled...

The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: Roche MODULAR ANALYTICS EVO Serum Work Area (SWA) Recalled by Roche...

The Issue: Under certain conditions loose ProCell/CleanCell aspiration tube filters may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: cobas 8000 analyzer series Operators Manual Roche cobas Filter label:...

The Issue: Under certain conditions loose ProCell/CleanCell aspiration tube filters may...

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

Class II — Potential Health HazardOngoing
DrugMay 20, 2014· West-Ward Pharmaceutical Corp.

Recalled Item: Isoniazid Tablets Recalled by West-Ward Pharmaceutical Corp. Due to Failed...

The Issue: Failed Dissolution Specifications: Stability lots cannot support dissolution...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 20, 2014· SCC Soft Computer

Recalled Item: SoftLab with SA HIS versions 4.0.7.0-4.0.7.1 SoftLab is a laboratory...

The Issue: The interface fails to send abnormal flags for Lab test results.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: ORTHO PACK EXTREMITY CUSTOMED CONTENTS: (1) TABLE COVER REINFORCED 50"...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: LAP Abdom w/pouch Customed code 900-2619 Recalled by Customed, Inc Due to...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: E..N.T. PACK - (5) SPONGE TONSIL 7/8 XRD (1) TABLE Recalled by Customed, Inc...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: Laparotomy Pack Recalled by Customed, Inc Due to Customed has determined...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: LAPAROSCOPY COLORECTAL SURGICAL PACK code 900-2259A Recalled by Customed,...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: LAPAROSCOPY PACK- - (1) DRAPE LAP ABDOMINAL WITH POUCH (1) Recalled by...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing