MOOG Curlin Infusion Administration Set — Class II medical device recall Z-0701-2018
Terminated recall by Zevex Incorporated (dba Moog Medical Medical Devices Group), reported 2018-03-07, distributed nationwide. Particulate found on the Curlin spike.
| Recall number | Z-0701-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zevex Incorporated (dba Moog Medical Medical Devices Group), Salt Lake City, UT, United States |
| Recall initiated | 2017-11-10 |
| Classified | 2018-02-23 |
| Reported by FDA | 2018-03-07 |
| Terminated | 2018-12-12 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, CA, HR, SA, TR |
| Reason classes | specification failure |
| UPC / GTIN / UDI-DI | 38148440000587 |
| Serial numbers | CF1517404, CF1519506, CF1521211, CF1522501, CF1526503, CF1530704, CF1611001, CF1618152 |
| Model numbers | 340-4168 |
Product
MOOG Curlin Infusion Administration Set, Ref 340-4168, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and distal Female Luer Y-Site with Check Valve, Anti-Siphon Valve included for Free Flow Protection, packaged 20/box, for use with the Moog Curlin Ambulatory Volumetric Infusion Pump, RX, Sterile. Product Usage: Administration set to be used with the Moog Curlin infusion Pump. The pump can be used for intravenous, intra-arterial, epidural, subcutaneous, or enteral infusions.
Reason for recall
Particulate found on the Curlin spike.
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-0701-2018. 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.