International safety notice
Lot recall of devices for BioFoam Surgical Matrix, CRYOLIFE
Germany / BfArM · DEU · Mar 10, 2014
Key facts
| Title | Lot recall of devices for BioFoam Surgical Matrix, CRYOLIFE |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | BioFoam Surgical Matrix, CRYOLIFE |
| Manufacturer | Lot recall of devices for BioFoam Surgical Matrix, CRYOLIFE |
| Models | 800-438-8285, 1063481-011714-001, 13BV005, 770-590-3781, 13BV004, BF1005, 13BV0005, BF005 |
| Date | Mar 10, 2014 |
| 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