International safety notice
Sistemas de drenaje torácico Pleur-evac®, Códigos de producto A-8000I y A-8000I-06
Spain / AEMPS · ESP · Jul 15, 2020
Key facts
| Title | Sistemas de drenaje torácico Pleur-evac®, Códigos de producto A-8000I y A-8000I-06 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistemas de drenaje torácico Pleur-evac®, Códigos de producto A-8000I y A-8000I-06 |
| Manufacturer | Teleflex Medical, Estados Unidos |
| Models | 74C2000474, 74F1500555, 74D1800632, 74C1800921, 74B1901993, 74B2000068, 74K1701305, 74E1701196, 74J1500223, 74A2002639, 74C1801548, 74J1902581 and 175 more |
| Event type | Safety Notice |
| Date | Jul 15, 2020 |
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