International safety notice
Recall for the CRIT-LINE® Blood Chamber, Fresenius USA Manufacturing, Inc.
Germany / BfArM · DEU · Jun 9, 2015
Key facts
| Title | Recall for the CRIT-LINE® Blood Chamber, Fresenius USA Manufacturing, Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the CRIT-LINE® Blood Chamber, Fresenius USA Manufacturing, Inc. |
| Manufacturer | Recall for the CRIT-LINE® Blood Chamber, Fresenius USA Manufacturing, Inc. |
| Models | 14091304, 14091314, 14091308, 14111303, 1-800-323-5188, 120305, 14111308, 15011308, 14061316, 14061301, 14031312, 14031205 and 328 more |
| Date | Jun 9, 2015 |
| 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