Quick Facts at a Glance
- Recall Date
- August 12, 2025
- Hazard Level
- HIGH
- Brand
- Applied Medical Technology
- Category
- Health & Personal Care
- Sold At
- Unknown
- Geographic Scope
- 2 states
- At-Risk Groups
- INFANTS, GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Applied Medical Technology
- Product type
- Nasal Feeding Tube with ENFit and Stylet
- Model numbers
- REF E NRT-05090-I, Box UDI (01)00842071149666(17)280601(10)250626-382, Pouch UDI: (01)00842071149543(17)280601(10)250620-245, Box UDI (01)00842071149666(17)280601(10)250623-271, Pouch UDI: (01)00842071149543(17)280601(10)250605-340, Box UDI (01)00842071149666(17)280501(10)250612-131, Pouch UDI: (01)00842071149543(17)280501(10)250529-090, (01)00842071149543(17)280501(10)250529-091 +4 more
- Sold at
- Unknown
- Where affected
- MA, RI
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
August 12, 2025
Reported by FDA DEVICE
October 15, 2025
RecallRadar source check
April 18, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Applied Medical Technology Inc or your healthcare provider for instructions. Notification method: Letter
About This Product
NutraGlide nasal feeding tubes are used to deliver nutrition, fluids, and medications through the nose into the stomach or intestine in neonatal, pediatric, and adult patients.
Why This Is Dangerous
A distal tip detachment can lead to partial or complete device failure and potential internal obstruction or injury.
Industry Context
This recall is not stated as part of a broader industry pattern.
Real-World Impact
The recall affects patients relying on nasal feeding tubes in clinical settings, with an emphasis on immediate action to stop use and consult providers.
Practical Guidance
How to identify if yours is affected
- Verify model number: REF E NRT-05090-I
- Check associated UDIs on the Box and Pouch
- Review recall notice for the exact lot or date codes
- If in doubt, cease use and contact the clinician or supplier
Where to find product info
Recall notice and enforcement details are available on the FDA enforcement page for Z-0128-2026.
What timeline to expect
Refund or replacement processing is typically 4-8 weeks after the recall resolution.
If the manufacturer is unresponsive
- Escalate to hospital risk management or patient safety office
- File a formal complaint with the device manufacturer
- Contact the FDA recall liaison if necessary
How to prevent similar issues
- Verify ENFit compatibility for future tubes
- Check UDIs and model numbers before use or purchase
- Keep recall notices and manufacturer guidance accessible
Documentation advice
Retain recall notices, serial or lot numbers, photos of the device, and all correspondence with the manufacturer.
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Reported Incidents
No injuries or incidents have been reported.
Key Facts
- Recall number Z-0128-2026
- Distributed to facilities in MA and RI
- Product: NutraGlide ENFit Nasal Feeding Tube with Stylet
- Model: REF E NRT-05090-I
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
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