Product Recalls in Missouri

Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,905 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,905 in last 12 months

Showing 2492124940 of 29,298 recalls

Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: IRK 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· Brainlab AG

Recalled Item: Navigation Spine & Trauma 3D Version 2.0 and 2.1 Is Recalled by Brainlab AG...

The Issue: Brainlab Navigation Software Spine & Trauma 3D 2.0/2.1 offers automatic...

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: System Manual 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: 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: 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· 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
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: Tummy Tuck Pack- FJG Recalled by Customed, Inc Due to Customed has...

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: 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
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: ARTHROSCOPY PACK I (1) CUSTOMED CONTENTS: (1) TOWELS ABSORBENT 15" Recalled...

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: PEDIATRIC LAP PACK - ( I) SHEET MINOR LAP 102" Recalled by Customed, Inc Due...

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: PREMIUM OPHTHALMIC PACK- CUSTOMED- (1) GOWN SMS X-LARGE STD RAGLAN Recalled...

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: FOLEY CATHETER KIT 1116FR. - CUSTOM ED- (1) WRAPPER 24" 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
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: ACDFPACK SURGICAL CENTER Recalled by Customed, Inc Due to Customed has...

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: UMBILICAL VESSEL CATHETER KIT - CUSTOMED- (1) PAPER TAPE MEASURE 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
Medical DeviceMay 20, 2014· Customed, Inc

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

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