FDA Device recall Z-0223-2023
NEO-fit Neonatal Endotracheal Tube Grip, Part Number 42-2540
- FDA Device
- Class II
- ongoing
- Published 2022-11-16
On 2022-11-16 the FDA classified a Class II recall of NEO-fit Neonatal Endotracheal Tube Grip, Part Number 42-2540 by Coopersurgical, citing firm has received 11 complaints involving a loose or detached metal clips, including 3 cases where the metal clip was ingested by the patient, and 3 cases where the metal clip was….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0223-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-10-20 |
| Published | 2022-11-16 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Coopersurgical |
| Distribution | US |
Product
NEO-fit Neonatal Endotracheal Tube Grip, Part Number 42-2540
Reason
Firm has received 11 complaints involving a loose or detached metal clips, including 3 cases where the metal clip was ingested by the patient, and 3 cases where the metal clip was removed from the patient's mouth. In one case, the patient suffered a laceration to the throat.
Identifiers
| code_info | Lot/Serial Number UDI-DI (GTIN-14 - not yet added to GUDID database) 272992 00888937016659 269476 00888937016659 269477…Lot/Serial Number UDI-DI (GTIN-14 - not yet added to GUDID database) 272992 00888937016659 269476 00888937016659 269477 00888937016659 269478 00888937016659 269479 00888937016659 269480 00888937016659 269482 00888937016659 269483 00888937016659 274957 00888937016659 274958 00888937016659 274960 00888937016659 274961 00888937016659 286859 00888937016659 286861 00888937016659 286863 00888937016659 292881 00888937016659 292883 00888937016659 292888 00888937016659 292889 00888937016659 292900 00888937016659 292901 00888937016659 292903 00888937016659 296236 00888937016659 296238 00888937016659 297033 00888937016659 297034 00888937016659 297035 00888937016659 298049 00888937016659 298055 00888937016659 298054 00888937016659 298056 00888937016659 298062 00888937016659 303771 00888937016659 303772 00888937016659 303950 00888937016659 304053 00888937016659 304363 00888937016659 305019 00888937016659 305020 00888937016659 307724 00888937016659 306339 00888937016659 306341 00888937016659 307728 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0223-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.