Zevex Incorporated (dba Moog Medical Medical Devices Group): Medical Device Recall in 2018 - (Recall #: Z-0699-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

MOOG Curlin Infusion Administration Set, Ref 340-4134, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and Y-Site with Check Valve, 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.

Product Classification:

Class II

Date Initiated: November 10, 2017

Date Posted: March 7, 2018

Recall Number: Z-0699-2018

Event ID: 78573

Reason for Recall:

Particulate found on the Curlin spike.

Status: Terminated

Product Quantity: 2,497/20-administration set cases

Code Information:

UDI 38148440000495, Lot/serial numbers: CF1518304, CF1521104, CF1524301, CF1523803, CF1528603, and CF1613101.

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.

Voluntary or Mandated:

Voluntary: Firm initiated