Z-0491-2012

McKESSON Medi-Pak Urethral Catheter Tray with Red Rubber Catheter Sterile.Single Use.Disposable 20 Trays Per...

Name: Z-0491-2012 McKESSON Medi-Pak Urethral Catheter Tray with Red Rubber Catheter Sterile.Single Use.Disposable 20 Trays Per...
Creator: Nurse Assist, Inc
Published: 2011-09-02
License: https://open.fda.gov/license/

Nurse Assist, LLC / initiated 2011-09-02 / Terminated / root cause: design

FDA source

Nurse Assist, Inc began a recall of McKESSON Medi-Pak Urethral Catheter Tray with Red Rubber Catheter Sterile.Single Use.Disposable 20 Trays Per Case Reorder No. 37-232 CAUTION: THIS PRODUCT... on 2011-09-02. The reason FDA records is "Nurse Assist, Inc. received a recall notice from the Triad Group. This recall has been initiated due to a recall of the PVP Solution Packs manufactured by the Triad Group that are contained in certain procedure trays". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number: Z-0491-2012
Status: Terminated
Initiated: 2011-09-02
Posted: 2012-01-11
Terminated: 2012-10-26
Recalling firm: Nurse Assist, LLC
Product: McKESSON Medi-Pak Urethral Catheter Tray with Red Rubber Catheter Sterile.Single Use.Disposable 20 Trays Per Case Reorder No. 37-232 CAUTION: THIS PRODUCT CONTAINS NATURAL RUBBER LATEX WHICH MAY CAUSE ALLERGIC REACTIONS Marketed by McKesson Corporation McKesson Medical-Surgical, Richmond, VA 23228 Made in the U.S.A. Urethral Catheter Tray with Red Rubber Catheter
Product code: KOD Catheter, Urological
Reason for recall: Nurse Assist, Inc. received a recall notice from the Triad Group. This recall has been initiated due to a recall of the PVP Solution Packs manufactured by the Triad Group that are contained in certain procedure trays.
Root cause tag: design
FDA root cause: Component design/selection
Action: Nurse Assist sent a recall notice dated September 2, 2011, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to examine their inventory immediately and quarantine the affected product. Customers were also instructed to identify their customers and notify them at once of the product recall. Customers were instructed to complete and return the enclosed response form as soon as possible. For those distributors that choose to destroy the affected product they must use the attached Notice of Destruction to report the specifics of the destroyed product. and contact Nurse Assist Customer Service for a RGA # prior to destruction. For any questions call Nurse Assist Customer Service at 1-800-649-6800.
Quantity in commerce: 13,928 cases
Distribution: Worldwide Distribution - USA (nationwide) and the countries of Canada and Saudi Arabia.
Product codes and lots: Assembly ID 37-232U. Lot Numbers: 902029, 902286, 904074, 905128, 906279, 907368, 908385, 909389, 911130, 912280, 1001222, 1003022, 1003390, 1004260, 1006033, 1007077, 1008230, 1009107, 1010077, and 1011135. Pack Lot #s: 34743, 34915, 35207, 35317, 33560, 35683, 35995, 36146, 36302, 36467, 36614, 36763, 36903, 37026, 37162, 37273, 37400, 37655, 37673, and 37807.

Product code KOD

K830359Class IISterile Catherization Procedure TraysWelcon, Inc. / cleared 1983-03-17

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 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)