Case Label: REORDER NO. 7200 (STERILE) CSR WRAP WELCON BRAND URETHRAL CATHETER TRAY w/o Catheter nurse assist incorporated 20 ex/Box 800-649-6800 3400 Northern Cross Blvd. Fort Worth, TX 76137 www.nurseassist.com Tray Label: REORDER NO. 7200 STERILE UNLESS OPENED OR DAMAGED nurse assist incorporated A6033, R1 SINGLE USE WELCON BRAND Urethral Catheter Tray Without Catheter 800-649-6800 3400 Northern Cross Blvd. Fort Worth, TX 76137 www.nurseassist.com LatexFree CONTENTS: CSR Wrap Waterproof Underpad Gloves Fenestrated Drape Forceps PVP Solution Rayon Balls in Prep Cup Specimen Container with ID Label Lube Jelly 1200 mL Graduated Drainage Tray Intended use: The trays are urological catheter trays.
FDA Recall Z-2265-2011 · Posted 2011-05-25
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Recalling FirmNurse Assist, Inc
Recall StatusTerminated
Product CodeKOD
Date Initiated2011-01-20
Date Terminated2012-10-25
Product Quantity441 cases
Reason for Recall
The trays contain Triad Group Sterile Lubricating Jelly packs recalled by Triad Group because of the possibility of inadequate sterilization.
Firm Action
The firm, Nurse Assist Incorporated, sent a letter dated January 20, 2011 to its customers. The letter described the product, problem and actions to be taken. The customers were instructed to examine their inventory immediately; quarantine the product; identify their customers and notify them at once about the product recall (Nurse Assist will provide bright labels to affix to your affected inventory); provide their customers with labels as well, and complete and return the attached RECALL ACKNOWLEGEMENT form via fax to: 817-231-1500 or mail to: Nurse Assist, Inc., 3400 Northern Cross Blvd., Forth Worth, TX 76137.
Only the product and lots identified on the attached list are affected.
If you have any questions or to request labels, please call Nurse Assist Customer Service Monday through Friday, from 8:00 am to 5:00 pm Central Time at 1-800-649-6800.
Root Cause
Other
Distribution Pattern
Worldwide distribution: USA (nationwide) and countries including: Canada, Dubai and Saudi Arabia.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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