Infinity Enteralite Ambulatory Feeding Pumps — Class II medical device recall Z-0764-2013
Terminated recall by MOOG Medical Devices Group, reported 2013-02-06, distributed nationwide. The firm is adding an addendum to the operator's manual for Infinity Enteralite Ambulatory Feeding Pumps perta
| Recall number | Z-0764-2013 |
|---|---|
| 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 | 2012-10-12 |
| Classified | 2013-01-31 |
| Reported by FDA | 2013-02-06 |
| Terminated | 2014-04-10 |
| Distributed | Nationwide (US) |
| Countries outside the US | DE, HR, LT |
| Quantity | 92,488 units |
| Serial numbers | 105061010, 105061013, 105061015, 105063004, 105063018, 105063019, 105063020, 105066004, 105066006, 105066015, 105066021, 105066023, 105066024, 105066028, 105066032, 105066036, 105066040, 105068002, 105068003, 105068005, 105068006, 105068007, 105068008, 105068009, 105068010 and 475 more |
Product
Infinity Enteralite Ambulatory Feeding Pumps, List number: INFKIT2 - Addendum to Operator's Manual Product usage: provide a means for the volumetric delivery of fluids used in Enteral applications.
Reason for recall
The firm is adding an addendum to the operator's manual for Infinity Enteralite Ambulatory Feeding Pumps pertaining to the Infinite Dose mode and the inability of the Pump to detect air in line.
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-0764-2013. 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.