Z-1003-04

Nasal Jejunal Feeding Tube, Tube Diameter: 10 FR. Tube Length: 240CM., Disposable Single Use Only, Rx...

Name: Z-1003-04 Nasal Jejunal Feeding Tube, Tube Diameter: 10 FR. Tube Length: 240CM., Disposable Single Use Only, Rx...
Creator: Wilson-Cook Medical Inc
Published: 2004-05-26
License: https://open.fda.gov/license/

Wilson-Cook Medical Inc. / initiated 2004-05-26 / Terminated / root cause: packaging

FDA source

Wilson-Cook Medical Inc began a recall of Nasal Jejunal Feeding Tube, Tube Diameter: 10 FR. Tube Length: 240CM., Disposable Single Use Only, Rx Only***COOK Wilson Cook Medical GI Endoscopy, 4900... on 2004-05-26. The reason FDA records is "The nasal transfer tube may be missing from the package of the affected lot". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as packaging.

Recall record

Recall number: Z-1003-04
Status: Terminated
Initiated: 2004-05-26
Posted: 2004-07-20
Terminated: 2004-09-14
Recalling firm: Wilson-Cook Medical Inc.
Product: Nasal Jejunal Feeding Tube, Tube Diameter: 10 FR. Tube Length: 240CM., Disposable Single Use Only, Rx Only***COOK Wilson Cook Medical GI Endoscopy, 4900 Bethania Station Road, Winston-Salem, NC 27105
Product code: FPD Tube, Feeding
Reason for recall: The nasal transfer tube may be missing from the package of the affected lot.
Root cause tag: packaging
FDA root cause: Other
Action: For the Domestic account, a recall letter was hand delivered by a Wilson-Cook representative on 5/26/2004. A letter was delivered via fax to International Distributors on 5/26/2004.
Quantity in commerce: 20 units
Distribution: NC, Ireland & Poland
Product codes and lots: Reorder/Catalog Number: NJFT-1-ML, Lot #1803299, Expiration Date: 09-2008

Product code FPD

K874393Class IIEnteral Feeding TubeWilson-Cook Medical, Inc. / cleared 1987-12-07

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)