Wilson-Cook Medical Inc. recalls Product Name: Nasal Jejunal Feeding Tube REF: NJFT-10
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-10UDI 108270022230183 affected lotsW4886945W488075010827002223018
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 detailsHide
International distribution to the country of Australia.
Use of the product may cause temporary or medically reversible adverse health consequences.
Sources & references
- FDA enforcement recordOfficial FDA database entry for Z-1298-2026
- FDA 510(k) clearance · K043203The device's official FDA premarket clearance record
- FDA device classification · KNTOfficial FDA classification for this device type
- CFR regulation · 21 CFR 876.5980The federal regulation governing this device
- FDA recall announcementSearch FDA.gov for the official press announcement
- Find Wilson-Cook Medical Inc.Search for the manufacturer's official notice
- News coverageRecent reporting on this recall and manufacturer
- openFDA data recordThe raw JSON record this page is built from
Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.
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.
More Class II recalls
Zimmer Surgical Inc recalls Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems S…
Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insignificant extension of surgery to find anot…
- Pneumatic Tourniquet
- Under Investigation by firm
Zimmer Surgical Inc recalls Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems D…
Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insignificant extension of surgery to find anot…
- Pneumatic Tourniquet
- Under Investigation by firm
W L Gore & Associates, Inc. recalls GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers (by Re…
Due to catheter separation
- Aortic Aneurysm Treatment Endovascular Graft System
- Under Investigation by firm
