International safety notice
Restylane SubQ Lidocaine
New Zealand / Medsafe Recalls · NZL · Mar 13, 2013
Key facts
| Regulator | New Zealand / Medsafe Recalls |
|---|---|
| Country | NZL |
| Brand | Restylane SubQ Lidocaine |
| Manufacturer | Q-Med AB |
| Event type | Recall |
| Action type | Recall - Unapproved medicine |
| Date | Mar 13, 2013 |
| 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