International safety notice
Lot recall of SpeediCath ® Compact Eve CH 12, Coloplast A/S
Germany / BfArM · DEU · May 24, 2016
Key facts
| Title | Lot recall of SpeediCath ® Compact Eve CH 12, Coloplast A/S |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot recall of SpeediCath ® Compact Eve CH 12, Coloplast A/S |
| Manufacturer | Lot recall of SpeediCath ® Compact Eve CH 12, Coloplast A/S |
| Models | 28112, 5107109, 5078049, 5081639, 01-04-2018, 5071034, 14-03-2016, DKTMD-2016-0426-2000, 5071032, 5081638, 5078051, 69749917 and 27 more |
| Date | May 24, 2016 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 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