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MOOG Medical Devices Group recalls ***This recall is being conducted due to an incomplete recall for RES 57829*** Curlin Infusion Administration Set, REF 3
Recalled October 24, 2012 · FDA recall Z-0072-2013 · MOOG Medical Devices Group
Hazard
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 · FDA Class II
Units
12,000 sets
Sold at
Nationwide Distribution including California
Description
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
Product
***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.
Manufacturer(s)
MOOG Medical Devices Group
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →