Z-1298-2026Class II

Product Name: Nasal Jejunal Feeding Tube REF: NJFT-10

Name: Z-1298-2026 Product Name: Nasal Jejunal Feeding Tube REF: NJFT-10
Creator: Wilson-Cook Medical Inc.
Published: 2025-12-15
License: https://open.fda.gov/license/

Wilson-Cook Medical Inc. / initiated 2025-12-15 / Open, Classified / root cause: manufacturing process

FDA source

Wilson-Cook Medical Inc. began a recall of Product Name: Nasal Jejunal Feeding Tube REF: NJFT-10 on 2025-12-15. FDA classified it as Class II and gives the reason as "Nasal feeding tube packaged without the nasal transfer tube component". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-1298-2026
Classification: Class II
Status: Open, Classified
Initiated: 2025-12-15
Posted: 2026-02-05
Recalling firm: Wilson-Cook Medical Inc.
Product: Product Name: Nasal Jejunal Feeding Tube REF: NJFT-10
Product code: KNT Tubes, Gastrointestinal (And Accessories)
Reason for recall: Nasal feeding tube packaged without the nasal transfer tube component.
Root cause tag: manufacturing process
FDA root cause: Employee error
Action: On January 5, 2026, Cook Endoscopy issued a Urgent Medical Device Recall Notification to affected consignees via E-Mail. Cook Endoscopy asked consignees to take the following actions: 1. Examine inventory immediately to determine if you have affected product(s). If so, quarantine any affected products that remain unused. Immediately cease all further distribution and use of the affected products. 2. Return the affected product(s) to Cook Medical with a signed copy of the Acknowledgement and Receipt Form. 3. Please complete the Acknowledgement and Receipt Form within 5 business days of receiving this letter regardless of whether you have affected product(s) on hand and email the completed form to [email protected]. 4. Please share this notice with appropriate personnel, including down to the user level, within your organization or with any organization where the potentially affected products have been transferred.
Quantity in commerce: 60 units
Distribution: International distribution to the country of Australia.
Product codes and lots: Lot Code:W4904253, W4886945, W4880750 UDI: 10827002223018

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1298-2026
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1298-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-02-11	2026-02-05

Product code KNT

K043203Class IIWilson-Cook Enteral Feeding Tube, Tiger Tube Enteral Feeding TubeWilson-Cook Medical, Inc. / cleared 2005-05-11

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)