International safety notice
Arrow® PICC (Peripherical Insertion Central Catether) y kits JACC (Jugular Axillo-subclavian Central Catheter) (Ver códigos del producto y lotes afectados en el anexo 2 de la nota de aviso de la empresa)
Spain / AEMPS · ESP · May 13, 2019
Key facts
| Title | Arrow® PICC (Peripherical Insertion Central Catether) y kits JACC (Jugular Axillo-subclavian Central Catheter) (Ver códigos del producto y lotes afectados en el anexo 2 de la nota de aviso de la empresa) |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Arrow® PICC (Peripherical Insertion Central Catether) y kits JACC (Jugular Axillo-subclavian Central Catheter) (Ver códigos del producto y lotes afectados en el anexo 2 de la nota de aviso de la empresa) |
| Manufacturer | Arrow International Inc., Estados Unidos |
| Models | 13F18D0384, 13F17H0110, 13F17F0107, 13F17F0099, 2019-250, 23F17J0249, 13F17F0109, 23F17L0593, PR-44052-BAS, 23F18E0352, 23F16L0434, 13F16H0359 and 77 more |
| Event type | Safety Notice |
| Date | May 13, 2019 |
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