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 in
Check against the official notice below — it lists the full affected range.
Zevex Incorporated is recalling the MOOG Curlin Infusion Administration Set (Ref 340-4134) due to particulate found on the Curlin spike. The affected product is a non-DEHP microbore tubing infusion set with a non-vented bag spike and Y-site with check valve. The recall involves 2,497 cases of 20-administration set units distributed nationwide in the United States, as well as to government, military, and foreign locations including Canada, Saudi Arabia, Turkey, Croatia, United Arab Emirates, and Australia. The recalled lots are identified by UDI 38148440000495 and the following lot/serial numbers: CF1518304, CF1521104, CF1524301, CF1523803, CF1528603, and CF1613101.
The recall notice does not specify a remedy or recommended action for consumers who may have received this product.
Written by software from the official notice below. Not reviewed by a lawyer.
Particulate found on the Curlin spike.
Reason for recall: Particulate found on the Curlin spike. Distribution: Distribution was nationwide. There was government and military distribution. Foreign distribution was made to Canada, Saudi Arabia, Turkey, Croatia, United Arab Emirates, and Australia. Quantity: 2,497/20-administration set cases Lot/code info: UDI 38148440000495, Lot/serial numbers: CF1518304, CF1521104, CF1524301, CF1523803, CF1528603, and CF1613101.
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.