Medline medical convenience kits labeled as: 1) NEONATAL INTUBATION… — Class I medical device recall Z-1505-2025
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2025-04-16, distributed in CA. Specific Medline Kits were manufactured using Intubation ORAL/NASAL Endotracheal Tubes which were subsequently
| Recall number | Z-1505-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2025-02-24 |
| Classified | 2025-04-10 |
| Reported by FDA | 2025-04-16 |
| Distributed | CA |
| Quantity | 1,550 units |
| UPC / GTIN / UDI-DI | 10193489218152, 10193489218169, 10193489268188, 10193489297980, 10193489457803, 10193489800944, 10193489922127, 10195327036980, 10195327153649, 10198459155765, 40193489218153, 40193489218160, 40193489268189, 40193489297981, 40193489800945, 40193489922128, 40195327036981, 40195327153640, 40198459155766 |
| Lot numbers | 20BDB854, 20BDC901, 20CDA453, 20CDA459, 20DDA921, 20EBC867, 20EBD635, 20EDB330, 20EDC042, 20FBJ920, 20FDA703, 20IDC153, 20LDA314, 20LDA466, 21ADB113, 21ADB162, 21BDB508, 21CDB435, 21HDB557, 21IDA608, 21JDA180, 21JDB271, 21KDA979, 21LDA450, 21LDB244, 22ADA311, 22BDA818, 22EDB187, 22FBF130, 22FDB822, 22HDB092, 22IBP405, 22IDA205, 22JDA908, 22KDA049, 22KDB696, 22LDA351, 23ADA938, 23CDA005, 23CDB015 and 12 more |
| Model numbers | ACC010371C, ACC010381A, ACC010381B, ACC010381C, ACC010395, ACC010397, ACC010541A, ACC010541B, ACC010541C, DYNJAA252 |
Product
Medline medical convenience kits labeled as: 1) NEONATAL INTUBATION TRAY, REF ACC010371C; 2) NEWBORN RESUSCITATION KIT, REF ACC010381A; 3) NEWBORN RESUSCITATION KIT, REF ACC010381B; 4) NEWBORN RESUSCITATION KIT, REF ACC010381C; 5) PEDS GREY-PINK-RED, REF ACC010395; 6) PEDS PURPLE, REF ACC010397; 7) NEONATAL INTUBATION TRAY, REF ACC010541A; 8) NEONATAL INTUBATION TRAY, REF ACC010541B; 9) NEONATAL INTUBATION TRAY, REF ACC010541C; 10) PEDIATRICS INTUBATION TRAY, REF DYNJAA252.
Reason for recall
Specific Medline Kits were manufactured using Intubation ORAL/NASAL Endotracheal Tubes which were subsequently recalled by Smiths Medical.
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-1505-2025. 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.