International safety notice
Urgent Field Safety Notice for Accu-Chek Inform II, cobas h 232 POC, CoaguChek Pro II, CoaguChek XS Plus/XS Pro by Roche Diagnostics GmbH
Germany / BfArM · DEU · Sep 10, 2018
Key facts
| Title | Urgent Field Safety Notice for Accu-Chek Inform II, cobas h 232 POC, CoaguChek Pro II, CoaguChek XS Plus/XS Pro by Roche Diagnostics GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Accu-Chek Inform II, cobas h 232 POC, CoaguChek Pro II, CoaguChek XS Plus/XS Pro |
| Manufacturer | Roche Diagnostics GmbH |
| Models | 04901126190, 04805658160, ≥KS04XXXXX, 04805658001, 07210841190, 04800842190, 03.01.06, SBN-CPS-2018-011, 05060311001, 05888760001, 14000, 03.06.00 and 17 more |
| Date | Sep 10, 2018 |
| 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