International safety notice
Lot Recall for the Duisburg Hollow Screw for Subdural Puncture, TELEFLEX
Germany / BfArM · DEU · May 14, 2012
Key facts
| Title | Lot Recall for the Duisburg Hollow Screw for Subdural Puncture, TELEFLEX |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Subdural Puncture, TELEFLEX |
| Manufacturer | Lot Recall for the Duisburg Hollow Screw for Subdural Puncture, TELEFLEX |
| Models | 07151, 406-566, LH1540N, 0172-8232078 |
| Date | May 14, 2012 |
| 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