International safety notice
Kit de cánula arterial EndoReturn. Nº de modelo: ER21B
Spain / AEMPS · ESP · Mar 17, 2023
Key facts
| Title | Kit de cánula arterial EndoReturn. Nº de modelo: ER21B |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Kit de cánula arterial EndoReturn. Nº de modelo: ER21B |
| Manufacturer | Edwards Lifesciences LLC, EEUU. |
| Models | 2023-127, 35002, 91122, 91.822.52.89, 28022, 46980, LOTE129488, FCA-177, ER21B, 129488 |
| Event type | Safety Notice |
| Date | Mar 17, 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