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U.S. Department of Health and Human Services

Class 2 Device Recall McKesson

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  Class 2 Device Recall McKesson see related information
Date Initiated by Firm January 20, 2011
Date Posted May 25, 2011
Recall Status1 Terminated 3 on October 25, 2012
Recall Number Z-2261-2011
Recall Event ID 58021
Product Classification Catheter, urological - Product Code KOD
Product Case Label: McKESSON Medi-Pak Uretheral Catheter Tray With Red Rubber Catheter Sterile Single Use Disposable 20 Trays Per Case Reorder No. 37-202 Marketed By McKesson Corporation McKesson Medical-Surgical, Richmond, VA 23228 Made in the U.S.A.

Tray label: McKesson Medi-Pak Urethral Catheter Tray With Red Rubber Catheter Sterile Single Use Disposable Contents: 1-14FR Red Rubber Catheter, 1-Pair of Vinyl Gloves, 1-Specimen Container with Lid and Label, 1-Fenestrated Drape, 1-Pack of PVP Solution, 1-Pack of Lubricating Jelly, 1-Pair of Forceps, 5-Rayon Balls in One Prep Cup, 1-Polylined Drape, 1-CSR Wrap, 1 Graduated Tray, 1200 cc Reorder No. 37-202 Contents STERILE In unopened, undamaged package. Marketed By McKesson Corporation McKesson Medical-Surgical, Richmond, VA 23228

Intended use: The trays are urological catheter trays.
Code Information Lot Codes: 809027, 812036, 901039, 902282, 903272, 903345, 906277, 908218, 909388, 911032, 912279, 1002027, 1003117, 1004345, 1006032, and 1007159
Recalling Firm/
Nurse Assist, Inc
3400 Northern Cross Blvd
Fort Worth TX 76137-3600
For Additional Information Contact
817-231-1300 Ext. 14
Manufacturer Reason
for Recall
The trays contain Triad Group Sterile Lubricating Jelly packs recalled by Triad Group because of the possibility of inadequate sterilization.
FDA Determined
Cause 2
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 1504 cases
Distribution Worldwide distribution: USA (nationwide) and countries including: Canada, Dubai and Saudi Arabia.
Total Product Life Cycle TPLC Device Report

1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.