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RecallWatchMedical Device Safety
Class IIOngoingZ-1298-2026

Wilson-Cook Medical Inc. recalls Product Name: Nasal Jejunal Feeding Tube REF: NJFT-10

Wilson-Cook Medical Inc.Winston Salem, NC, United StatesReported Feb 11, 2026 · 5 months ago
Legal News Analyst ·

Reason for recall

Nasal feeding tube packaged without the nasal transfer tube component.

Affected product

Check your device

Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.

Affected products & lots

  • Product Name: Nasal Jejunal Feeding Tube REF:NJFT-10
    UDI 10827002223018
    3 affected lots
    W4886945W488075010827002223018

What the firm is doing

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 ausrecalls@cookmedical.com. 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.

DistributionShow details

International distribution to the country of Australia.

Class IIWhat this means

Use of the product may cause temporary or medically reversible adverse health consequences.

Sources & references

Taylor Coteus
Legal News Analyst

Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.

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