International safety notice
600005
New Zealand / Medsafe Recalls · NZL · May 21, 2019
Key facts
| Title | 600005 |
|---|---|
| Regulator | New Zealand / Medsafe Recalls |
| Country | NZL |
| Brand | Curved Artery Forceps Single Use |
| Manufacturer | Jimy Brothers Group |
| Models | 600005 |
| Event type | Recall |
| Action type | Recall |
| Date | May 21, 2019 |
| Regulator page | medsafe.govt.nz |
At a glance
- Yes Recall
- No Field safety notice
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