International safety notice
Recall for dual Lumen Catheter, Gyrus ACMI Inc.
Germany / BfArM · DEU · Jul 29, 2008
Key facts
| Title | Recall for dual Lumen Catheter, Gyrus ACMI Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | dual Lumen Catheter, Gyrus ACMI Inc. |
| Manufacturer | Recall for dual Lumen Catheter, Gyrus ACMI Inc. |
| Models | 804.2624, 7269089, 608BX, 8031030, 7361043, 7347078, 8017047, 7306089, 7303068, 888-524-7266, 8066067, 7324062 and 35 more |
| Date | Jul 29, 2008 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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