Moog Curlin Infusion — Class II medical device recall Z-0688-2016
Terminated recall by MOOG Medical Devices Group, reported 2016-02-17, distributed nationwide. Moog is recalling Curlin 4000, 6000, and PainSmart Infusion Pumps manufactured or serviced by MMDG between Mar
| Recall number | Z-0688-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | MOOG Medical Devices Group, Salt Lake City, UT, United States |
| Recall initiated | 2015-12-23 |
| Classified | 2016-02-11 |
| Reported by FDA | 2016-02-17 |
| Terminated | 2017-02-21 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, HR, IT, JP, KR, NZ, SA, TR |
| Quantity | 11,472 |
| Model numbers | 340, 340-4038, 360 |
Product
Moog Curlin Infusion, Ambulatory Infusion Pump The Curlin Ambulatory Infusion System includes Curlin Ambulatory multi-therapy and PainSmart pumps. Curlin 4000, catalog number 340; Curlin 6000, 6000 CMS, and PainSmart IOD, catalog number 360; and Curlin Pump Calibration Set, catalog number 340-4038.
Reason for recall
Moog is recalling Curlin 4000, 6000, and PainSmart Infusion Pumps manufactured or serviced by MMDG between March 18, 2015 and November 6, 2015 because the master pumps used to calibrate them were out of tolerance and may cause an over delivery of medications and solutions at a rate of 1.2 - 6.8% faster than programmed.
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-0688-2016. 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.