International safety notice
Accesorios de VHK y VKMO(D) Adult/Small Adult, fabricados después del 4 de marzo de 2019. Ver referencias afectadas en la nota de aviso de la empresa
Spain / AEMPS · ESP · Sep 30, 2019
Key facts
| Title | Accesorios de VHK y VKMO(D) Adult/Small Adult , fabricados después del 4 de marzo de 2019. Ver referencias afectadas en la nota de aviso de la empresa |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Accesorios de VHK y VKMO(D) Adult/Small Adult , fabricados después del 4 de marzo de 2019. Ver referencias afectadas en la nota de aviso de la empresa |
| Manufacturer | Maquet Cardiopulmonary GmbH, Alemania |
| Models | 92268504, 92283543, 92272095, 701067951, 51000, 76437, 92282198, 70000, 701067968, 91.822.52.89, 701067962, 2019-530 and 38 more |
| Event type | Safety Notice |
| Date | Sep 30, 2019 |
At a glance
- No Recall
- Yes Field safety notice
- 1,000+ Matching device models in FDA data
- 100–999 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