Zevex Incorporated (dba MOOG Medical Devices Group)
Zevex Incorporated (dba MOOG Medical Devices Group) appears in FDA public data with 2 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2053-2019, Class II) was initiated on February 27, 2019.
Summary
- Total Recalls
- 2
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-2053-2019 | Class II | MOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with Non-Vented Bag Spike and | February 27, 2019 |
| Z-2054-2019 | Class II | MOOG Curlin Infusion Administration Set, REF 340-4130-V, Non-DEHP Tubing with Non-Vented Bag Spike a | February 27, 2019 |