International safety notice
Pulsavac® Plus Wound Debridement System and Pulsavac® Plus AC Wound Debridement System
Ireland / HPRA · IRL · Aug 1, 2019
Key facts
| Title | Pulsavac® Plus Wound Debridement System and Pulsavac® Plus AC Wound Debridement System |
|---|---|
| Regulator | Ireland / HPRA |
| Country | IRL |
| Brand | Pulsavac® Plus Wound Debridement System and Pulsavac® Plus AC Wound Debridement System |
| Manufacturer | Zimmer Biomet |
| Models | 30296159, Z000012722, 30296161, 28372669, ZFA2019-00062, 29020056, Z000012609, Z000012267, 31070782, 29370088, 29020139, CP04102 and 88 more |
| Event type | Recall |
| Date | Aug 1, 2019 |
| Regulator page | hpra.ie |
At a glance
- Yes Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1