International safety notice
Recall of the product Urgo Aphthen, Urgo GmbH
Germany / BfArM · DEU · Oct 1, 2012
Key facts
| Title | Recall of the product Urgo Aphthen, Urgo GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the product Urgo Aphthen, Urgo GmbH |
| Manufacturer | Recall of the product Urgo Aphthen, Urgo GmbH |
| Models | DE13B26511, 18914.1, 579-212, COBADEFF590, 579-0, DE138265119, 66272, D-66280, UST..1DCNTNUMMOC, 04011, 24.09.2012, 21150070 and 3 more |
| Date | Oct 1, 2012 |
| 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