International safety notice
Recall for Hydromax, Carl Zeiss Meditec
Germany / BfArM · DEU · Aug 18, 2010
Key facts
| Title | Recall for Hydromax, Carl Zeiss Meditec |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Hydromax, Carl Zeiss Meditec |
| Manufacturer | Recall for Hydromax, Carl Zeiss Meditec |
| Models | 1058045201077660020038, HM1207004505, 17053, 23.5D, TARNFR2L, 524T-N, 10558NS201077660020038, HM1207004500, BRP0710, 26.5D, HM1207004504, HM1207004508 and 1 more |
| Date | Aug 18, 2010 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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