FDA Device recall Z-0764-2013

Infinity Enteralite Ambulatory Feeding Pumps, List number: INFKIT2 - Addendum to Operator's Manual Product usage: provide a means for the v…

FDA Device
Class II
terminated
Published 2013-02-06

On 2013-02-06 the FDA classified a Class II recall of Infinity Enteralite Ambulatory Feeding Pumps, List number: INFKIT2 - Addendum to Operator's Manual Product usage: provide a means for the v… by Moog Medical Devices Group, citing 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 dete….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0764-2013
Classification	Class II
Status	terminated
Initiated	2012-10-12
Published	2013-02-06
Last updated	2026-09-13 11:53 UTC
Company	Moog Medical Devices Group
Distribution	US

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

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.

Identifiers

code_info	List number: INFKIT2 Lot/Serial numbers: 105068015, 105068002, 105068014, 105068013, 105068012, 105068011, 105068009,… List number: INFKIT2 Lot/Serial numbers: 105068015, 105068002, 105068014, 105068013, 105068012, 105068011, 105068009, 105068008, 105068007, 105066024, 105066021, 105068003, 105068005, 105068006, 105066004, 105068027, 105068028, 105068026, 105068019, 105068020, 105068031, 105068037, 105068023, 105068025, 105068034, 105068018, 105068017, 105068016, 105068033, 105068032, 105068030, 105068029, 105068036, 105068035, 105068022, 105068038, 105069005, 105069004, 105069003, 105069002, 105069001, 105069008, 105069007, 105069006, 105068039, 105068040, 105068041, 105069009, 105069014, 105069013, 105069012, 105069010, 105069011, 105070009, 105070008, 105070001, 105070010, 105070011, 105070003, 105070004, 105070005, 105070006, 105070007, 105069024, 105069023, 105069018, 105069025, 105069017, 105070002, 105069015, 105080001, 105070012, 105070013, 105070015, 105070016, 105070017, 105070018, 105070019, 105070020, 105070021, 105070022, 105080004, 105080002, 105081007, 105081027, 105081033, 105081002,

code_info

List number: INFKIT2 Lot/Serial numbers: 105068015, 105068002, 105068014, 105068013, 105068012, 105068011, 105068009,…

List number: INFKIT2 Lot/Serial numbers: 105068015, 105068002, 105068014, 105068013, 105068012, 105068011, 105068009, 105068008, 105068007, 105066024, 105066021, 105068003, 105068005, 105068006, 105066004, 105068027, 105068028, 105068026, 105068019, 105068020, 105068031, 105068037, 105068023, 105068025, 105068034, 105068018, 105068017, 105068016, 105068033, 105068032, 105068030, 105068029, 105068036, 105068035, 105068022, 105068038, 105069005, 105069004, 105069003, 105069002, 105069001, 105069008, 105069007, 105069006, 105068039, 105068040, 105068041, 105069009, 105069014, 105069013, 105069012, 105069010, 105069011, 105070009, 105070008, 105070001, 105070010, 105070011, 105070003, 105070004, 105070005, 105070006, 105070007, 105069024, 105069023, 105069018, 105069025, 105069017, 105070002, 105069015, 105080001, 105070012, 105070013, 105070015, 105070016, 105070017, 105070018, 105070019, 105070020, 105070021, 105070022, 105080004, 105080002, 105081007, 105081027, 105081033, 105081002,

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-0764-2013%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.