International safety notice
Anclaje de sutura FOOTSPRINT Ultra PK, 4,5 mm, referencia 72202901, y Anclaje de sutura FOOTSPRINT Ultra PK, 5,5 mm, referencia 72202902
Spain / AEMPS · ESP · Apr 3, 2020
Key facts
| Title | Anclaje de sutura FOOTSPRINT Ultra PK, 4,5 mm, referencia 72202901, y Anclaje de sutura FOOTSPRINT Ultra PK, 5,5 mm, referencia 72202902 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Anclaje de sutura FOOTSPRINT Ultra PK, 4,5 mm, referencia 72202901, y Anclaje de sutura FOOTSPRINT Ultra PK, 5,5 mm, referencia 72202902 |
| Manufacturer | Smith & Nephew, Inc, Endoscopy Division, EEUU. |
| Models | 2017849, 2016234, 2030940, 2023273, 2033663, 50730870, 2027398, 2017819, 2033523, 2038310, 2025169, 2022264 and 102 more |
| Event type | Safety Notice |
| Date | Apr 3, 2020 |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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