***This recall is being conducted due to an incomplete recall for RES… — Class II medical device recall Z-0072-2013
Terminated recall by MOOG Medical Devices Group, reported 2012-10-24, distributed nationwide. This recall is the same issue for the FDA processed recall initiated by Moog Medical Devices on 1/25/11 which
| Recall number | Z-0072-2013 |
|---|---|
| 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 | 2012-09-26 |
| Classified | 2012-10-17 |
| Reported by FDA | 2012-10-24 |
| Terminated | 2013-04-05 |
| Distributed | Nationwide (US) |
| Quantity | 12,000 sets |
| Lot numbers | 340-4128-V/CRF10082001, 340-4165/CF1022905, 340-4166/CF1022906 |
| Model numbers | 340-4165 |
Product
***This recall is being conducted due to an incomplete recall for RES 57829*** Curlin Infusion Administration Set, REF 340-4165, Sterile EO, The Curlin Ambulatory Infusion Pump System with disposable PVC Administration Tubing Sets and user accessories, provide a means for the volumetric delivery of fluids used in Parenteral, Enteral, Epidural, Subcutaneous and Intravenous applications.
Reason for recall
This recall is the same issue for the FDA processed recall initiated by Moog Medical Devices on 1/25/11 which was related to customers reporting unclearable Air-In-Line alarm with specific lot numbers of Curlin Administration Sets used with Curlin Ambulatory Infusion Pumps. The lots associated with this recall were inadvertently omitted from the original recall which has since been terminated by
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-0072-2013. 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.