Data Foundry

Medical device recalls 2012

EnteraLite Infinity Enteral Feeding Pump identified with the… — Class II medical device recall Z-0294-2013

Terminated recall by MOOG Medical Devices Group, reported 2012-11-21, distributed nationwide. MOOG Medical Devices Group is conducting a voluntary for a limited set of serial numbers of the EnteraLite Inf

Recall numberZ-0294-2013
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmMOOG Medical Devices Group, Salt Lake City, UT, United States
Recall initiated2012-11-08
Classified2012-11-15
Reported by FDA2012-11-21
Terminated2014-01-30
DistributedNationwide (US)
Countries outside the USCA, LT
Quantity8,736
Serial numbers506249031, 506264096, 506272024, 506335006, 506335145, 506336089, 506336096, 506362083, 506362086, 507018037, 507018060, 507067220, 507085140, 507087018, 507087140, 507095089, 507095171, 507121102, 507122050, 507122066, 507123149, 507123163, 507144016, 507144057, 507144215 and 475 more

Product

EnteraLite Infinity Enteral Feeding Pump identified with the following list numbers: INFKIT2 and INFORNG. The device is used with disposable PVC administration tubing sets to provide a means for the volumetric delivery of fluids used in enteral applications. The EnteraLite Infinity enteral feeding pump with disposable PVC administration tubing sets and user accessories provide a means for the volumetric delivery of fluids used in enteral applications.

Reason for recall

MOOG Medical Devices Group is conducting a voluntary for a limited set of serial numbers of the EnteraLite Infinity and Infinity Orange Small Volume Enteral Feeding Pumps because certain diodes on the PCB assembly may result in insufficient voltage to a portion of the pump resulting in an error 13 message and shutting the pump down entirely.

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-0294-2013. 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.