Z-2266-2011

Case Label: REORDER NO. 7201 (STERILE) CSR WRAP WELCON BRAND URETHRAL CATHETER TRAY w/ Plastic Catheter...

Name: Z-2266-2011 Case Label: REORDER NO. 7201 (STERILE) CSR WRAP WELCON BRAND URETHRAL CATHETER TRAY w/ Plastic Catheter...
Creator: Nurse Assist, Inc
Published: 2011-01-20
License: https://open.fda.gov/license/

Nurse Assist, LLC / initiated 2011-01-20 / Terminated / root cause: sterility

FDA source

Nurse Assist, Inc began a recall of Case Label: REORDER NO. 7201 (STERILE) CSR WRAP WELCON BRAND URETHRAL CATHETER TRAY w/ Plastic Catheter anureses assist incorporated 20 ea/Box 800-649-6800... on 2011-01-20. The reason FDA records is "The trays contain Triad Group Sterile Lubricating Jelly packs recalled by Triad Group because of the possibility of inadequate sterilization". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as sterility.

Recall record

Recall number: Z-2266-2011
Status: Terminated
Initiated: 2011-01-20
Posted: 2011-05-25
Terminated: 2012-10-25
Recalling firm: Nurse Assist, LLC
Product: Case Label: REORDER NO. 7201 (STERILE) CSR WRAP WELCON BRAND URETHRAL CATHETER TRAY w/ Plastic Catheter anureses assist incorporated 20 ea/Box 800-649-6800 3400 Northern Cross Blvd. Fort Worth, TX 76137 www.nurseassist.com Tray Label: REORDER NO. 7201 SINGLE USE/STERILE UNLESS OPENED OR DAMAGED Accorde Urethral Catheter Tray with Plastic Catheter CONTENTS: CSR wrap Underpad Gloves Fenestrated drape Forceps PVP Solution Rayon balls in prep cup Specimen container and label Lube jelly Graduated tray Plastic Catheter Another cost effective product from Welcon, Inc. Providence, RI 02909 Intended use: The trays are urological catheter trays.
Product code: KOD Catheter, Urological
Reason for recall: The trays contain Triad Group Sterile Lubricating Jelly packs recalled by Triad Group because of the possibility of inadequate sterilization.
Root cause tag: sterility
FDA root cause: Other
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.
Quantity in commerce: 64 cases
Distribution: Worldwide distribution: USA (nationwide) and countries including: Canada, Dubai and Saudi Arabia.
Product codes and lots: Lot Codes: 901043 and 905132.

Product code KOD

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)