International safety notice
Urgent Field Safety Notice for ARCHITECT c4000 / c8000 / c16000 cuvette segments by Abbott Laboratories
Germany / BfArM · DEU · Feb 7, 2018
Key facts
| Title | Urgent Field Safety Notice for ARCHITECT c4000 / c8000 / c16000 cuvette segments by Abbott Laboratories |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ARCHITECT c4000 / c8000 / c16000 cuvette segments |
| Manufacturer | Abbott Laboratories |
| Models | C8000, 02P75‐01, C4000, 75038‐4313, 01G46‐01, 1‐877‐4ABBOTT, C16000, 09D32‐05 |
| Date | Feb 7, 2018 |
| 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