Product Recalls in Arizona

Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 959 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
959 in last 12 months

Showing 43701–43720 of 52,339 recalls

Medical DeviceMay 21, 2014· Becton Dickinson & Co.

Recalled Item: BBL CrystaLEAD Enteric/Nonfermentor (E/NF) Identification (ID) System...

The Issue: A portion of the BBL Crystal Enteric/Nonfermentor (E/NF) Identification kits...

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

Class III — Low RiskOngoing
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: 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· 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: 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 6000 analyzer series Operators Manual Roche cobas 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· 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· 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· 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· 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· 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 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: 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: 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 20, 2014· Customed, Inc

Recalled Item: CYSTO TUR PACK BASIC CODE 900-2899. CONTENTS: (2) LEGGINGS W/7'' 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: EAR PACK CONTENTS: (I) CAUTERY PENC IL ROCKER SW I 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: IMPLANTE DE ORTHOPEDIA - ( I) CAUTERY T IP POLI 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: FACE PACK AESTHETIC SURGERY AESTHETIC SURGERY CONTENTS: (15) APPLICATOR...

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: ENDOVENOUS CUSTOM PACK - CUSTOMED (1) SYRINGE 5cc WITHOUT NEEDLE 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