Device recall: This recall is being conducted due to an incomplete recall for RES 57829 Curlin Infusion Administration Set, REF…

Class II FDA enforcement event 63359. Recall start date: 26 Sep 2012. Status in the FDA record: Terminated. Termination date: 5 Apr 2013.

Reason for recall, in the words of FDA

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

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

MOOG Medical Devices Group started this device recall on 26 Sep 2012. The firm address in the FDA record is in Salt Lake City, UT. FDA put the recall in Class II. FDA event 63359 has 1 product record. The first FDA enforcement report date is 24 Oct 2012. The record gives the status Terminated, with the termination date 5 Apr 2013.

FDA enforcement report The 1 product record

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on 1 Oct 2026. openFDA export of 28 Sep 2026.

Distribution

In the words of FDA.

Nationwide Distribution including California

Recalling firm

MOOG Medical Devices Group, Salt Lake City, UT.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

1 product record in the event.

FDA event 63359: product records
Recall number	Product	Quantity	Class	Status	Report date
Z-0072-2013	*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…	12,000 sets	Class II	Terminated	24 Oct 2012

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class II: The middle of the three FDA recall classes.

The event in context

Device events that started in 2012: 823
Share of these events in Class II: 88%
Product records in this event: 1Median of the firm: 1
Events of the firm on the register: 5

Other events of the firm

Other FDA enforcement events of MOOG Medical Devices Group
Initiated	Product (first record)	Type	Class	Records
23 Dec 2015	Moog Curlin Infusion, Ambulatory Infusion Pump The Curlin Ambulatory Infusion System includes Curlin Ambulatory multi-th	Device	Class II	1
20 Nov 2015	Catalog No. INF0020-A – EnteraLite Infinity Enteral Pump Delivery Set with ENFit Connector System and Transitional Stepp	Device	Class II	1
8 Nov 2012	EnteraLite Infinity Enteral Feeding Pump identified with the following list numbers: INFKIT2 and INFORNG. The device is	Device	Class II	1
12 Oct 2012	Infinity Enteralite Ambulatory Feeding Pumps, List number: INFKIT2 - Addendum to Operator's Manual Product usage: provid	Device	Class II	1

MOOG Medical Devices Group: all 5 events

Official channels

FDA enforcement report Z-0072-2013The FDA record of the first product of this event.
FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
FDA MedWatchThe FDA safety reporting program for drugs and medical devices.

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Cite this page

Recall Register. FDA enforcement event 63359. https://recallregister.com/fda/ii/63359/. Source: openFDA enforcement reports. Data through 28 Sep 2026.

Sources

Source: openFDA device enforcement reports
Licence: CC0 1.0
Export date: 28 Sep 2026
Newest FDA report date on the register: 23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?: The FDA record gives this distribution: Nationwide Distribution including California
What quantity of product is in FDA event 63359?: The FDA record gives this quantity: 12,000 sets
How did the recall start?: The FDA record says: Voluntary: Firm initiated
How many device recalls of 2012 have the same class?: 88% of the 823 device events that started in 2012 are in Class II.