International safety notice
Recall for several products because of a packaging error, Angiotech
Germany / BfArM · DEU · Sep 17, 2009
Key facts
| Title | Recall for several products because of a packaging error, Angiotech |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | several products because of a packaging error, Angiotech |
| Manufacturer | Recall for several products because of a packaging error, Angiotech |
| Models | 竈1111竈, R鬧, 338.0440, 1800.338.0662, 800.333.0440, 1홯ILL, 11111111111, 용民-회D8, 수튀1회V, •&11E화?, 352.338.0662, 5§磊§르글류전蔓 and 4 more |
| Date | Sep 17, 2009 |
| 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