International safety notice
BiPAP A30, BiPAP A30 EFL, BiPAP A30 Hybrid, BiPAP A40, BiPAP A40 EFL, BiPAP A40 Pro.
Spain / AEMPS · ESP · Jul 8, 2024
Key facts
| Title | BiPAP A30, BiPAP A30 EFL, BiPAP A30 Hybrid, BiPAP A40, BiPAP A40 EFL, BiPAP A40 Pro. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | BiPAP A30, BiPAP A30 EFL, BiPAP A30 Hybrid, BiPAP A40, BiPAP A40 EFL, BiPAP A40 Pro. |
| Manufacturer | Respironics, Inc, EEUU. |
| Models | 15668, 28050, 91.822.52.89, 00088, 28500, 28022, 28670, 2023-CC-SRC-039-B, 104647, 36418, 08009, 28703 and 3 more |
| Event type | Safety Notice |
| Date | Jul 8, 2024 |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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