Zevex Incorporated (dba Moog Medical Medical Devices Group)
Zevex Incorporated (dba Moog Medical Medical Devices Group) appears in FDA public data with 6 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0701-2018, Class II) was initiated on November 10, 2017.
Summary
- Total Recalls
- 6
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-0701-2018 | Class II | MOOG Curlin Infusion Administration Set, Ref 340-4168, Non-DEHP Microbore Tubing with Non-Vented Bag | November 10, 2017 |
| Z-0699-2018 | Class II | MOOG Curlin Infusion Administration Set, Ref 340-4134, Non-DEHP Microbore Tubing with Non-Vented Bag | November 10, 2017 |
| Z-0697-2018 | Class II | MOOG Curlin Infusion Administration Set, Ref 340-4114, Non-DEHP Microbore Tubing with Non-Vented Bag | November 10, 2017 |
| Z-0698-2018 | Class II | MOOG Curlin Infusion Administration Set, Ref 340-4133, Non-DEHP Microbore Tubing with Non-Vented Bag | November 10, 2017 |
| Z-0700-2018 | Class II | MOOG Curlin Infusion Administration Set, Ref 340-4166, Non-DEHP Microbore Tubing with Non-Vented Spi | November 10, 2017 |
| Z-0702-2018 | Class II | MOOG Curlin Infusion Administration Set, Ref 340-4169, Non-DEHP Microbore Tubing with Non-Vented Bag | November 10, 2017 |