Data Foundry

Medical device recalls 2018

NeoMed Enteral Feeding Tubes with Enteral Only Connectors — Class II medical device recall Z-0093-2019

Terminated recall by Neomed Inc, reported 2018-10-17, distributed nationwide. Potential for the tethered plug on the hub of the NeoMed Enteral Feeding Tubes with Enteral Only Connectors to

Recall numberZ-0093-2019
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmNeomed Inc, Woodstock, GA, United States
Recall initiated2018-06-04
Classified2018-10-09
Reported by FDA2018-10-17
Terminated2020-07-21
DistributedNationwide (US)
Countries outside the USAU, CA, ES, MX, SG
Lot numbers20170721, 20170804, 20170813, 20170904, 20170914, 20170915, 20170918, 20170919, 20171006, 20171009, 20171011, 20171018, 20171019, 20171020, 20171114, 20171122, 20171128, 20171130, 20171202, 20171204, 20171207, 20171209, 20171214, 20171216, 20171219, 20171222, 20171227, 20171230, 20180103, 20180108, 20180111, 20180113, 20180116, 20180122, 20180202, 20180205, 20180208, 20180303, 20180309, FTL5.0PEO and 13 more
Model numbers20170721, 20170804, 20170813, 20170904, 20170914, 20170915, 20170918, 20170919, 20171006, 20171009, 20171011, 20171018, 20171019, 20171020, 20171114, 20171122, 20171128, 20171130, 20171202, 20171204, 20171207, 20171209, 20171214, 20171216, 20171219 and 28 more

Product

NeoMed Enteral Feeding Tubes with Enteral Only Connectors, French sizes 4.0Fr, 5.0Fr, 6.5Fr, 8.0Fr, and lengths 40cm, 60cm, 90cm. The product consists of a polyurethane feeding tube with an attached hub and tethered plug to close the hub when the feeding tube is not in use. Product Usage: Intended for use in neonatal and pediatric patients to provide nutrition via nasal or oral gastric placement and is not intended for use beyond 30 days.

Reason for recall

Potential for the tethered plug on the hub of the NeoMed Enteral Feeding Tubes with Enteral Only Connectors to inadvertently open after closure.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0093-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.