International safety notice
Recall of several batches of the product family Tissue-Guard (Vascu-Guard, Dura-Guard, Peri-Guard and Supple-Peri-Guard), Synovis/Baxter
Germany / BfArM · DEU · May 2, 2014
Key facts
| Title | Recall of several batches of the product family Tissue-Guard (Vascu-Guard, Dura-Guard, Peri-Guard and Supple-Peri-Guard), Synovis/Baxter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of several batches of the product family Tissue-Guard (Vascu-Guard, Dura-Guard, Peri-Guard and Supple-Peri-Guard), Synovis/Baxter |
| Manufacturer | Recall of several batches of the product family Tissue-Guard (Vascu-Guard, Dura-Guard, Peri-Guard and Supple-Peri-Guard), Synovis/Baxter |
| Models | DURAWGUARDJ4X4CM, 321301100011, SPCE113-04D0101, FEB0071, FEB0026, SPCE11303C0038, O.8X8CM, 04D0104, DURA-GUARDßX8CM, 321406080011, 321301060011, 796.7300 and 111 more |
| Date | May 2, 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