International safety notice
Accu-chek® Inform II, CoaguChek Pro II system, CoaguChek® XS Plus system, CoaguChek® XS Plus system, CoaguChek® XS Pro system, cobas h 232 POC system, cobas h 232 POC system (scanner version)
Spain / AEMPS · ESP · Sep 20, 2018
Key facts
| Title | Accu-chek® Inform II , CoaguChek Pro II system, CoaguChek® XS Plus system, CoaguChek® XS Plus system, CoaguChek® XS Pro system, cobas h 232 POC system, cobas h 232 POC system (scanner version) |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Accu-chek® Inform II , CoaguChek Pro II system, CoaguChek® XS Plus system, CoaguChek® XS Plus system, CoaguChek® XS Pro system, cobas h 232 POC system, cobas h 232 POC system (scanner version) |
| Manufacturer | Roche Diagnostics GmbH, Alemania. |
| Models | 14000, 05530199190, 04901142190, 03.01.04, B61503355, ≥KQ03XXXXX, 04901126190, 2018-492, T30354, 03.01.03, 03.06.00, 07210841190 and 20 more |
| Event type | Safety Notice |
| Date | Sep 20, 2018 |
At a glance
- No Recall
- Yes 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