International safety notice
Corrective action for the Vitek 2 Piperacillin/Tazobactam Test, Biomerieux
Germany / BfArM · DEU · Apr 21, 2011
Key facts
| Title | Corrective action for the Vitek 2 Piperacillin/Tazobactam Test, Biomerieux |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Vitek 2 Piperacillin/Tazobactam Test, Biomerieux |
| Manufacturer | Corrective action for the Vitek 2 Piperacillin/Tazobactam Test, Biomerieux |
| Models | 410023, 22355, AST-N183, AST-N145, 22269, AST-GN41, AST-N080, AST-N138, AST-GN24, 22253, AST-N174, 22295 and 224 more |
| Date | Apr 21, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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