International safety notice
Lot Recall for Prostaflow catheters, Coloplast
Germany / BfArM · DEU · Dec 13, 2010
Key facts
| Title | Lot Recall for Prostaflow catheters, Coloplast |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Prostaflow catheters, Coloplast |
| Manufacturer | Lot Recall for Prostaflow catheters, Coloplast |
| Models | 10050408, 10051713, 10051704, 10051708, 10051476, 10060826, 10070404, 10062934, 10061652, 10051489, 10050402, 10071912 and 74 more |
| Date | Dec 13, 2010 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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