Nasal Feeding Tube Recall: NutraGlide with Stylet ENFit
The NutraGlide Nasal Feeding Tube with Stylet and ENFit is being recalled because its distal tips may detach at lower than expected forces. About 390 units were distributed in the US, specifically to Massachusetts and Rhode Island, and the recall is categorized as moderate severity by the FDA. The corrective action is not specified.
| Brand | Applied Medical Technology Inc |
|---|---|
| Product | NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 90, REF E NRT-05090-I The NutraGlide Nasal Feeding Tube is a feeding tube placed through the nose and ending in the stomach or intestine used for the administration of nutrition, fluids, and medications in neonatal, pediatric, and adult patients. |
| Reason | The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces. |
| Severity | moderate |
| Units affected | 390 units |
| Distribution | US distribution to MA and RI |
| Agency | FDA |
WHAT YOU SHOULD DO
- Stop using the recalled NutraGlide nasal feeding tube.
- Contact your healthcare provider or medical device supplier for guidance and possible replacement.
- Do not reuse or modify the device; keep it and its packaging with you for reference.
- Follow disposal or return instructions from your clinician or supplier and report any related problems.
How to identify the recalled item
| Lot / date codes | 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, (01)00842071149543(17)280501(10)250529-092, (01)00842071149543(17)280501(10)250529-093, (01)00842071149543(17)280501(10)250529-094, (01)00842071149543(17)280501(10)250529-095. |
|---|---|
| Lot / date codes | Box P/N NFT-06090-I, Lot Number 250825-220, exp. 2028-04-01, UDI (01)00842071149161(17)280401(10)250825-220, Pouch P/N ENFT-06090-I, Lot Number 250812-459, exp. 2028-04-01, UDI (01)00842071149086(17)280401(10)250812-459; Box P/N NFT-06090-I, Lot Number 250821-277, exp. 2028-04-01, UDI (01)00842071149161(17)280401(10)250821-277, Pouch P/N ENFT-06090-I, Lot Number 250812-453, exp. 2028-04-01, UDI (01)00842071149086(17)280401(10)250812-453; Box P/N NFT-06090-I, Lot Number 250815-364, exp. 2028-04-01, UDI (01)00842071149161(17)280401(10)250815-364, Pouch P/N ENFT-06090-I, Lot Number 250812-458, exp. 2028-04-01, UDI (01)00842071149086(17)280401(10)250812-458. |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.