RecallHawk
Class II Recall

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

Wilson-Cook Medical Inc.

Summary

The FDA issued a Class II for Product Name: Nasal Jejunal Feeding Tube REF: NJFT-10 by Wilson-Cook Medical Inc.. Reason: Nasal feeding tube packaged without the nasal transfer tube component..

Details

Source

Device Recall

External ID

Z-1298-2026

Action Date

2026-02-11

Status

Ongoing

Category

device

Product Description

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

Lot/Code Info: Lot Code:W4904253, W4886945, W4880750 UDI: 10827002223018

Quantity Affected: 60 units

Reason for Recall

Nasal feeding tube packaged without the nasal transfer tube component.

Distribution

International distribution to the country of Australia.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-12-15

Company

Wilson-Cook Medical Inc.

Winston Salem, NC

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 207 device recalls issued in the same week, part of 403 device-related FDA actions this month.

Wilson-Cook Medical Inc. has 19 FDA actions in our database, including 16 recalls and 3 clearances.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Wilson-Cook Medical Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Wilson-Cook Medical Inc. have FDA actions?

Wilson-Cook Medical Inc. has 19 FDA actions in our database, including 16 recalls and 3 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "Z-1298-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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