International safety notice
HLS Set Advanced 7.0 con recubrimiento BIOLINE (referencia: BE-HLS 7050); HLS Set Advanced 5.0 con recubrimiento BIOLINE (referencia: BE-HLS 5050); HLS Set Advanced 7.0 con recubrimiento SOFLINE (referencia: BO-HLS 7050)
Spain / AEMPS · ESP · Jul 27, 2022
Key facts
| Title | HLS Set Advanced 7.0 con recubrimiento BIOLINE (referencia: BE-HLS 7050) ; HLS Set Advanced 5.0 con recubrimiento BIOLINE (referencia: BE-HLS 5050); HLS Set Advanced 7.0 con recubrimiento SOFLINE (referencia: BO-HLS 7050) |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | HLS Set Advanced 7.0 con recubrimiento BIOLINE (referencia: BE-HLS 7050) ; HLS Set Advanced 5.0 con recubrimiento BIOLINE (referencia: BE-HLS 5050); HLS Set Advanced 7.0 con recubrimiento SOFLINE (referencia: BO-HLS 7050) |
| Manufacturer | Maquet Cardiopulmonary GmbH, Alemania |
| Models | 82072, 28521, 2022-367, 2022-07-01, 04058863005744, 3000189274, 3000220053, 3000227602, 04058863078298, 3000227600, 01-11-2020, 3000182107 and 13 more |
| Event type | Safety Notice |
| Date | Jul 27, 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