CLASS II ONGOING Device recall · Reported 11 Feb 2026 · FDA Enforcement Report

Nasal Jejunal Feeding Tube recalled by Wilson-Cook Medical

Wilson-Cook Medical is recalling Nasal Jejunal Feeding Tube, distributed nationwide in the US. The recall was initiated on 15 Dec 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Code:W4904253, W4886945, W4880750 UDI: 10827002223018

Quantity recalled60 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1298-2026
FDA event ID: 98274
Recalling firm: Wilson-Cook Medical, Winston Salem, NC
Classification: Class II
Status: Ongoing
Recall initiated: 15 Dec 2025
FDA classified: 5 Feb 2026
Reported: 11 Feb 2026
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Packaging Defects
Device type: Other Medical Devices

Timeline

15 Dec 2025	Recall initiated by company
5 Feb 2026	Classified by FDA	+52 days
11 Feb 2026	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Nasal feeding tube packaged without the nasal transfer tube component.

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

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

Where it was distributed

International distribution to the country of Australia.

Nationwide

Questions about this recall

Is Nasal Jejunal Feeding Tube recalled?

Yes. Wilson-Cook Medical recalled Nasal Jejunal Feeding Tube on 15 Dec 2025. The recall is Class II and its status is Ongoing. Recall number Z-1298-2026.

Why was it recalled?

Nasal feeding tube packaged without the nasal transfer tube component.

Which lots are affected?

Lot Code:W4904253, W4886945, W4880750 UDI: 10827002223018

Where was it sold?

International distribution to the country of Australia.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Wilson-Cook Medical

All 23

Reported	Class	Recall	Company	Reason	Where
22 Apr 2026Device	CLASS II	Instinct Plus Endoscopic Clipping Device recalled by Wilson-Cook Medical	Wilson-Cook Medical	Sterility	Nationwide
25 Feb 2026Device	CLASS II	Teslatome Bipolar Sphincterotomes recalled by Wilson-Cook Medical	Wilson-Cook Medical	Other	4 states
11 Dec 2024Device	CLASS II	Cook Medical Hemo-7-EU Hemospray Endoscopic Hemostat recalled	Wilson-Cook Medical	Sterility	NC
23 Oct 2024Device	CLASS II	Cook Medical Hemo-7 Hemospray Endoscopic Hemostat recalled	Wilson-Cook Medical	Sterility	Nationwide
13 Dec 2023Device	CLASS II	Quantum Ttc Biliary Balloon Dilator recalled by Wilson-Cook Medical	Wilson-Cook Medical	Other	NC

Other Other Medical Devices recalls

All 13,778

Reported	Class	Recall	Company	Reason	Where
16 Sep 2026Device	CLASS II	Citric Complete Dry Citric Acid Concentrate recalled	Nipro Renal Soultions USA	Other	Nationwide
16 Sep 2026Device	CLASS I	Kit: Epidural/Pain TQC 20/Cs recalled by Medical Action Industries	Medical Action Industries Inc. 306	Sterility	6 states
16 Sep 2026Device	CLASS II	Halyard IV Start Kit Non-Sterile recalled by Avid Medical	Avid Medical	Sterility	Nationwide
16 Sep 2026Device	CLASS I	Kit: Single Shot Epidural 20/Cs recalled by Medical Action Industries	Medical Action Industries Inc. 306	Sterility	6 states
16 Sep 2026Device	CLASS II	AMS Convenience Kit: Dsaek Pack - RX recalled	Windstone Medical Packaging	Device Malfunction	Nationwide