MOOG Medical Devices Group: Medical Device Recall in 2012 - (Recall #: Z-0072-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

***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 Parenteral, Enteral, Epidural, Subcutaneous and Intravenous applications.

Product Classification:

Class II

Date Initiated: September 26, 2012

Date Posted: October 24, 2012

Recall Number: Z-0072-2013

Event ID: 63359

Reason for Recall:

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

Status: Terminated

Product Quantity: 12,000 sets

Code Information:

Product Code/Lot Number: 340-4166/CF1022906; 340-4128-V/CRF10082001; 340-4165/CF1022905.

Distribution Pattern:

Nationwide Distribution including California

Voluntary or Mandated:

Voluntary: Firm initiated