International safety notice
Lot Recall of the user-specific Foliodrape CombiSets for ophthalmologic surgery, Paul Hartmann AG
Germany / BfArM · DEU · Mar 10, 2011
Key facts
| Title | Lot Recall of the user-specific Foliodrape CombiSets for ophthalmologic surgery, Paul Hartmann AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ophthalmologic surgery, Paul Hartmann AG |
| Manufacturer | Lot Recall of the user-specific Foliodrape CombiSets for ophthalmologic surgery, Paul Hartmann AG |
| Models | 100304, 400910, 269680, 0001145274, 1011036, ZUR0CK, 0001644272, 4008003, 100211, MS3I1, 1011040, 000925273 and 24 more |
| Date | Mar 10, 2011 |
| 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