Food, drugs, devices › Wilson-Cook Medical Inc.

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

FDA enforcement event 98274 · Class II · initiated 15 Dec 2025 · status Ongoing

DeviceVoluntary: Firm initiated1 product recordWinston Salem, NC

FDA enforcement event 98274 is a device recall by Wilson-Cook Medical Inc. of Winston Salem, NC, initiated 15 Dec 2025 and classified Class II, with 1 product record.

FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 85% of the 945 device enforcement events initiated in 2025 carry the same class.

Status: Ongoing. Initiation: voluntary: firm initiated. Wilson-Cook Medical Inc. has 14 enforcement events on this register, with a median of 1 product record per event.

Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.

Recalling firm

Wilson-Cook Medical Inc., Winston Salem, NC.

Reason for recall

"Nasal feeding tube packaged without the nasal transfer tube component."

Distribution

"International distribution to the country of Australia."

Product records

Recall number	Product	Quantity	Class	Status	Report date
Z-1298-2026	Product Name: Nasal Jejunal Feeding Tube REF: NJFT-10	60 units	Class II	Ongoing	11 Feb 2026

Context

85%of 2025 device events are Class II945 events that year

1product record in this eventfirm median: 1

14events on this register for the firm

Other enforcement events for Wilson-Cook Medical Inc.

Initiated	Product (first record)	Type	Class	Records
20 Aug 2026	Brand Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Product Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Model/Catalog Number: HEMO-7, HEMO	Device	Class II	1
3 Mar 2026	Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO	Device	Class II	1
18 Dec 2025	Teslatome Bipolar Sphincterotomes REF: TESLA-B2535-260 Model Number: G60784 UDI-DI code: 00827002607842 REF: TESLA-B2535	Device	Class II	1
31 Oct 2024	Cook Medical HEMO-7-EU Hemospray Endoscopic Hemostat, REF G24663, 2.8 cm, sterile.	Device	Class II	1
29 Aug 2024	Cook Medical Hemo-7 Hemospray Endoscopic Hemostat, REF G56572, 2.8 mm, Sterile; and Hemo-10 Hemospray Endoscopic Hemosta	Device	Class II	1
3 Nov 2023	QUANTUM TTC BILIARY BALLOON DILATOR, REF QBD-10X3, Order Number G22657; used to dilate strictures of the biliary tree	Device	Class II	7
22 Jun 2023	Fusion Lithotripsy Extraction Basket, Model Number FS-LXB-2X4 G48277; Fusion Lithotripsy Extraction Baskets are intended	Device	Class II	2
22 May 2023	Hemospray Endoscopic Hemostat: Reference Part Numbers: a) HEMO-7, REF G56572; b) HEMO-7-EU, REF G24663;	Device	Class II	2
4 Feb 2020	HEMO-7 Hemospray Endoscopic Hemostat	Device	Class II	2
24 Jul 2019	Hemospray Endoscopic Hemostat	Device	Class II	1

All 14 events for Wilson-Cook Medical Inc.

Questions and answers

Why was this device recalled?

FDA's record gives the reason for recall as: "Nasal feeding tube packaged without the nasal transfer tube component."

What does Class II mean?

FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.

Where was the product distributed?

FDA's distribution pattern field reads: "International distribution to the country of Australia."

Is the recall still ongoing?

FDA lists the status as Ongoing. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.

Where does this data come from?

openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.

Provenance

Source: openFDA device enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.