International safety notice
Lot Recall for ReNu® Multi-Purpose Solution, Bausch & Lomb
Germany / BfArM · DEU · Jan 11, 2011
Key facts
| Title | Lot Recall for ReNu® Multi-Purpose Solution, Bausch & Lomb |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ReNu® Multi-Purpose Solution, Bausch & Lomb |
| Manufacturer | Lot Recall for ReNu® Multi-Purpose Solution, Bausch & Lomb |
| Models | F9114, 09143, G9124, C9161, M9022, E9028, D9069, F9045, C9088, F9047, 09048, D9068 and 38 more |
| Date | Jan 11, 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