International safety notice
Batch recall of SwiveLock SP Suture Anchor, Arthrex GmbH
Germany / BfArM · DEU · Apr 10, 2017
Key facts
| Title | Batch recall of SwiveLock SP Suture Anchor, Arthrex GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Batch recall of SwiveLock SP Suture Anchor, Arthrex GmbH |
| Manufacturer | Batch recall of SwiveLock SP Suture Anchor, Arthrex GmbH |
| Models | 10078258, 10072425, 10084027, 10074288, 10077133, AR-2323PSLM, 85235, 10075965, AR-2600SBS-7, 10073992, 10078340, 10077252 and 13 more |
| Date | Apr 10, 2017 |
| Regulator page | bfarm.de |
At a glance
- No 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