International safety notice
Recall of combination disks cefpodoxime/clavulanate, Oxoid
Germany / BfArM · DEU · Feb 16, 2005
Key facts
| Title | Recall of combination disks cefpodoxime/clavulanate, Oxoid |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of combination disks cefpodoxime/clavulanate, Oxoid |
| Manufacturer | Recall of combination disks cefpodoxime/clavulanate, Oxoid |
| Models | 27.01.05, 3291857, 858793, 463388, 1612B, 368726, 1596B, 012561, 01256, D-46467, CT1596B |
| Date | Feb 16, 2005 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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