International safety notice
Recall for ProcedurePak products, Mölnlycke Health Care
Germany / BfArM · DEU · Apr 13, 2012
Key facts
| Title | Recall for ProcedurePak products, Mölnlycke Health Care |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ProcedurePak products, Mölnlycke Health Care |
| Manufacturer | Recall for ProcedurePak products, Mölnlycke Health Care |
| Models | 50034768, 94705, 94706 |
| Date | Apr 13, 2012 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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