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Recall Observatory FDA recall evidence

Device product

MOOG Curlin Infusion Administration Set, Ref 340-4169, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and distal Ultrasite Needleless Injection Port (Positive Pressure), Anti-Siphon Valve included for Free Flow Protection, packaged 20/box, for use with the Moog Curlin Ambulatory Volumetric Infusion Pump, RX, Sterile. Product Usage: Administration set to be used with the Moog Curlin infusion Pump. The pump can be used for intravenous, intra-arterial, epidural, subcutaneous, or enteral infusions.

Z-0702-2018

November 10, 2017

Class II

Product summary

Firm
Zevex Incorporated (dba Moog Medical Medical Devices Group)
Event
Event 78573
Status
Terminated
Classification
Class II
Quantity
785/20-administration set cases
Official record key
device-enforcement:Z-0702-2018

Official wording

Reason: Particulate found on the Curlin spike.

Code information: UDI 38148440000594, Lot/serial numbers: CF1520208, CF1522301, and CF1532971.

Distribution pattern: Distribution was nationwide. There was government and military distribution. Foreign distribution was made to Canada, Saudi Arabia, Turkey, Croatia, United Arab Emirates, and Australia.

Derived failure modes

  • Foreign material or chemical contamination

    reason.foreign_material_chemical_contamination · v1.0.0

    Particulate