FDA Device recall Z-0294-2013
EnteraLite Infinity Enteral Feeding Pump identified with the following list numbers: INFKIT2 and INFORNG. The device is used with disposabl…
- FDA Device
- Class II
- terminated
- Published 2012-11-21
On 2012-11-21 the FDA classified a Class II recall of EnteraLite Infinity Enteral Feeding Pump identified with the following list numbers: INFKIT2 and INFORNG. The device is used with disposabl… by Moog Medical Devices Group, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0294-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-11-08 |
| Published | 2012-11-21 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Moog Medical Devices Group |
| Distribution | US |
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
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.
Identifiers
| code_info | INFKIT2 with serial numbers: 506249031, 506264096, 506272024, 506335006, 506335145, 506336089, 506336096, 506362083, 50…INFKIT2 with serial numbers: 506249031, 506264096, 506272024, 506335006, 506335145, 506336089, 506336096, 506362083, 506362086, 507018037, 507018060, 507067220, 507085140, 507087018, 507087140, 507095089, 507095171, 507121102, 507122050, 507122066, 507123149, 507123163, 507144016, 507144057, 507144215, 507144220, 507144221, 507144226, 507151002, 507155019, 507155021, 507155094, 507155127, 507155156, 507155159, 507156065, 507157048, 507157124, 507164009, 507173005, 507173019, 507173063, 507179123, 507180064, 507186018, 507186098, 507186176, 507197012, 507197024, 507197036, 507201013, 507201038, 507205054, 507206064, 507212012, 507212013, 507214065, 507214098, 507214162, 507215041, 507218016, 507219057, 507219087, 507219103, 507220106, 507221098, 507227116, 507229033, 507229039, 507229060, 507232030, 507236063, 507236203, 507236303, 507239056, 507241089, 507242130, 507242201, 507247049, 507248031, 507248087, 507248095, 507249131, 507250175, 507255025, 507257123, 507257129, 507261065, 507 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0294-2013%22
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