International safety notice
Recall of normed TWIST DRILL cannulated / normed-V-TEK TWIST DRILL cannulated, Zimmer Biomet / Zimmer GmbH
Germany / BfArM · DEU · Jun 28, 2016
Key facts
| Title | Recall of normed TWIST DRILL cannulated / normed-V-TEK TWIST DRILL cannulated, Zimmer Biomet / Zimmer GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of normed TWIST DRILL cannulated / normed-V-TEK TWIST DRILL cannulated, Zimmer Biomet / Zimmer GmbH |
| Manufacturer | Recall of normed TWIST DRILL cannulated / normed-V-TEK TWIST DRILL cannulated, Zimmer Biomet / Zimmer GmbH |
| Models | 502015621, ST502015640, 502015628, ST502015620, ST502015635, 502015620, 502015629, 502015640, 502015635, 2016-07, ST502015621, CANN1 and 1 more |
| Date | Jun 28, 2016 |
| Regulator page | bfarm.de |
At a glance
- No 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