HIGH

Applied Medical Technology Recalls Nasal Feeding Tubes Due to Detachment Hazard

Applied Medical Technology recalled 1,780 NutraGlide Nasal Feeding Tubes on August 12, 2025, after reports of distal tips detaching. This recall affects tubes distributed in Massachusetts and Rhode Island. The detachment poses a high risk for patients requiring enteral nutrition.

Quick Facts at a Glance

Recall Date
August 12, 2025
Hazard Level
HIGH
Brand
Applied Medical Technology
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
2 states
At-Risk Groups
GENERAL

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

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Product Details

The recall includes NutraGlide Nasal Feeding Tubes with Stylet and ENFit, sizes 5 F - 6 F x 55, REF E NRT-05055-I. These tubes were distributed in the US, specifically in Massachusetts and Rhode Island.

The Hazard

The distal tips of the NutraGlide Nasal Feeding Tubes may detach at lower than expected forces. This defect poses a significant risk to patients who depend on these feeding tubes for nutrition, fluids, and medications.

Reported Incidents

There have been no reported injuries or incidents associated with this recall. The potential for detachment remains a serious concern for patient safety.

What to Do

Patients and healthcare providers should stop using the NutraGlide Nasal Feeding Tubes immediately. Follow the recall instructions provided by Applied Medical Technology Inc. Contact the manufacturer or your healthcare provider for further instructions.

Contact Information

For more information, contact Applied Medical Technology Inc. at [insert phone number]. Additional details can be found on their website or through the FDA recall notice.

Key Facts

  • Recall date: August 12, 2025
  • Quantity recalled: 1,780 units
  • Distribution limited to MA and RI
  • High hazard level due to potential detachment

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Model Numbers
REF E NRT-05055-I
Affected States
MA, RI
Report Date
October 15, 2025
Source Agency
FDA - Medical Devices
Recall Status
ACTIVE

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