Zevex Incorporated (dba MOOG Medical Devices Group) Recalls

FDA
1
Total Recalls
1
Agencies
Apr 2021
First Recall
Apr 2021
Latest Recall

Showing 1-1 of 1 recalls

FDA

MOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter, packaged 20 sets/carton, 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.

Administration sets leaked at the filter.

The recalling firm issued a letter dated 2/27/2019 via regular mail on 2/272019 to their direct accounts describing the issue, risk to health, and the necessary actions to be taken.