International safety notice
Bombas de infusión Sapphire: Sapphire Multi-Therapy (Nº modelo 15031-000-0008) y Sapphire Epidural (Nº modelo 15032-000-0003)
Spain / AEMPS · ESP · Oct 2, 2023
Key facts
| Title | Bombas de infusión Sapphire: Sapphire Multi-Therapy (Nº modelo 15031-000-0008) y Sapphire Epidural (Nº modelo 15032-000-0003) |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Bombas de infusión Sapphire: Sapphire Multi-Therapy (Nº modelo 15031-000-0008) y Sapphire Epidural (Nº modelo 15032-000-0003) |
| Manufacturer | Eitan Medical Ltd., Israel |
| Models | AP205, 30036-7655, 30036-7659, 30036-7501, 30036-7993, 30036-7947, 30036-7647, 38002-5720, 38002-7557, 36022-8425, AP237, 30041-2171 and 133 more |
| Event type | Safety Notice |
| Date | Oct 2, 2023 |
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