International safety notice
01520218S|12106450S|18060050S|18060080S|18060083S|18060084S|18060085S|18060090S|18060093S|1806125oS|18061417S|18063030S|18063031S
New Zealand / Medsafe Recalls · NZL · Jan 5, 2016
Key facts
| Title | 01520218S|12106450S|18060050S|18060080S|18060083S|18060084S|18060085S|18060090S|18060093S|1806125oS|18061417S|18063030S|18063031S |
|---|---|
| Regulator | New Zealand / Medsafe Recalls |
| Country | NZL |
| Brand | Stryker Guide Wires and K-Wires for T2 and gamma Systems |
| Manufacturer | Stryker Trauma AG |
| Models | 18060090S, 18060093S, 18060083S, 18060050S, 18060084S, 18063030S, 18060080S, 18060085S, 1806125OS, 18061417S, 01520218S, 12106450S and 1 more |
| Event type | Recall |
| Action type | Recall |
| Date | Jan 5, 2016 |
| Regulator page | medsafe.govt.nz |
At a glance
- Yes Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers 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