MOOG Curlin Infusion Administration Set — Class II medical device recall Z-2054-2019
Terminated recall by Zevex Incorporated (dba MOOG Medical Devices Group), reported 2019-07-31, distributed in GA, IL, KS, MA, MI, OH. Administration sets leaked at the filter.
| Recall number | Z-2054-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zevex Incorporated (dba MOOG Medical Devices Group), Salt Lake City, UT, United States |
| Recall initiated | 2019-02-27 |
| Classified | 2019-07-23 |
| Reported by FDA | 2019-07-31 |
| Terminated | 2021-04-28 |
| Distributed | GA, IL, KS, MA, MI, OH |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 38148440000471 |
| Lot numbers | CF1820216, CF1821617, CF1822214, CF1823616 |
| Model numbers | 340-4130-V |
Product
MOOG Curlin Infusion Administration Set, REF 340-4130-V, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter with add-on check valve, packaged 20 sets/carton, sterile. The firm name on the label is ZEVEX, Inc., Salt Lake City, UT.
Reason for recall
Administration sets leaked at the filter.
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-2054-2019. 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.