International safety notice
Sistemas de bomba de infusión CME/BD BodyGuard
Spain / AEMPS · ESP · Dec 11, 2023
Key facts
| Title | Sistemas de bomba de infusión CME/BD BodyGuard |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistemas de bomba de infusión CME/BD BodyGuard |
| Manufacturer | Caesarea Medical Electronics Limited, Reino Unido. |
| Models | 2021-494, 323BODYGUARD™, 545BODYGUARD™, 2021-494.LA, 575BODYGUARD™, 100384, 2023-563, 28022, IL-MF-000030321, 28750, 91.822.52.89, MMS-21-4135 |
| Event type | Safety Notice |
| Date | Dec 11, 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