International safety notice
Urgent Field Safety Notice for Atellica and ADVIA Creatine Kinase (CK_L) Reagent by Siemens Healthcare Diagnostics Inc. Tarrytown
Germany / BfArM · DEU · May 21, 2019
Key facts
| Title | Urgent Field Safety Notice for Atellica and ADVIA Creatine Kinase (CK_L) Reagent by Siemens Healthcare Diagnostics Inc. Tarrytown |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Atellica and ADVIA Creatine Kinase (CK_L) Reagent |
| Manufacturer | Siemens Healthcare Diagnostics Inc. Tarrytown |
| Models | 468449, ACHC19, 2018-08-01, 2019-09-01, 465336, 280767, 471332, 280765, 10591, ACHC19-02.A.OUS.ACHC, 11097640, 10729780 and 11 more |
| Date | May 21, 2019 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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