International safety notice
AXIOM Sensis, Combo 64 IECG, 6623974. AXIOM Sensis, Hemo LOW, 6634633. AXIOM Sensis, Combo 32 IECG, 6634641. AXIOM Sensis, EP 129 IECG, 6634658. Sensis, 10764561. Sensis Lite, 10764562. Sensis Vibe Combo, 11007642.
Spain / AEMPS · ESP · Aug 8, 2022
Key facts
| Title | AXIOM Sensis, Combo 64 IECG, 6623974. AXIOM Sensis, Hemo LOW, 6634633. AXIOM Sensis, Combo 32 IECG, 6634641. AXIOM Sensis, EP 129 IECG, 6634658. Sensis, 10764561. Sensis Lite, 10764562. Sensis Vibe Combo, 11007642. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | AXIOM Sensis, Combo 64 IECG, 6623974. AXIOM Sensis, Hemo LOW, 6634633. AXIOM Sensis, Combo 32 IECG, 6634641. AXIOM Sensis, EP 129 IECG, 6634658. Sensis, 10764561. Sensis Lite, 10764562. Sensis Vibe Combo, 11007642. |
| Manufacturer | Siemens Healthcare GmbH, Alemania |
| Models | 28022, AXA5-200.623.63.02.04, 6634641, 28906, 91.822.52.89, 6634658, 2022-388, AX033, 6623974.AXIOM, 11007642, 10764562, 10764562.SENSIS and 10 more |
| Event type | Safety Notice |
| Date | Aug 8, 2022 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 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