International safety notice
TEG® 5000 Reactivo de Fibrinógeno Funcional, referencia 07-034
Spain / AEMPS · ESP · Feb 22, 2023
Key facts
| Title | TEG® 5000 Reactivo de Fibrinógeno Funcional, referencia 07-034 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | TEG® 5000 Reactivo de Fibrinógeno Funcional, referencia 07-034 |
| Manufacturer | Haemonetics Corporation, EE.UU. |
| Models | FF0690, HMO5568, FF0660, HMO5650, FSCA-FY23-06, FF0740, 90383, 2023-077, 28022, FF0680, HMO5482, HMO5651 and 8 more |
| Event type | Safety Notice |
| Date | Feb 22, 2023 |
At a glance
- No Recall
- Yes 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