International safety notice
Corrective Action concerning Oxoid Columbia Agar with Sheep Blood PLUS PB 5039 A (Lot- No: 1262841) due to a microbial contamination, OXOID
Germany / BfArM · DEU · Dec 17, 2012
Key facts
| Title | Corrective Action concerning Oxoid Columbia Agar with Sheep Blood PLUS PB 5039 A (Lot- No: 1262841) due to a microbial contamination, OXOID |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Corrective Action concerning Oxoid Columbia Agar with Sheep Blood PLUS PB 5039 A (Lot- No: 1262841) due to a microbial contamination, OXOID |
| Manufacturer | Corrective Action concerning Oxoid Columbia Agar with Sheep Blood PLUS PB 5039 A (Lot- No: 1262841) due to a microbial contamination, OXOID |
| Models | 1262841, 17871, 46483, PB5039A |
| Date | Dec 17, 2012 |
| 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