Salt Lake City, UT, United States
Zevex Incorporated (dba MOOG Medical Devices Group) recalls
1 recall recorded since 2018, most recently on 27 February 2019. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 27 February 2019
- Terminated
- 28 April 2021
- Reason
- Administration sets leaked at the filter.
- Distribution
- Distribution was made to GA, IL, KS, MA, MI, and OH. There was no foreign/military/government distribution.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-2053-2019, Z-2054-2019
- 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 M
- MOOG Curlin Infusion Administration Set, REF 340-4130-V, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter with add-on check valve, packaged 20 sets/carton, sterile. The firm name on the label is ZE
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.