International safety notice
Lot Recall for Hydrolift spine implants, AESCULAP
Germany / BfArM · DEU · Sep 23, 2010
Key facts
| Title | Lot Recall for Hydrolift spine implants, AESCULAP |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Hydrolift spine implants, AESCULAP |
| Manufacturer | Lot Recall for Hydrolift spine implants, AESCULAP |
| Models | 21060, 51660087, 51651709, SV012T, 2010-08-26, 00036, 726261, 78501, 2010—09—13, 78532, 51654664, 51653357 and 10 more |
| Date | Sep 23, 2010 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 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