International safety notice
Equipo de stent ureteral Kwart Retro-Inject™, nº referencia 003500, 003600, 003700, 003800, AQ-003500, AQ-003600, AQ-003700; Equipo de stent de pieloplastia intraoperatoria Salle, nº referencia SIPSF-040018-56-6, SIPSF-040018-59, SIPSF-050018-59
Spain / AEMPS · ESP · May 3, 2019
Key facts
| Title | Equipo de stent ureteral Kwart Retro-Inject™, nº referencia 003500, 003600, 003700, 003800, AQ-003500, AQ-003600, AQ-003700; Equipo de stent de pieloplastia intraoperatoria Salle, nº referencia SIPSF-040018-56-6, SIPSF-040018-59, SIPSF-050018-59 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Equipo de stent ureteral Kwart Retro-Inject™, nº referencia 003500, 003600, 003700, 003800, AQ-003500, AQ-003600, AQ-003700; Equipo de stent de pieloplastia intraoperatoria Salle, nº referencia SIPSF-040018-56-6, SIPSF-040018-59, SIPSF-050018-59 |
| Manufacturer | Cook Incorporated, Estados Unidos |
| Models | G14837, G14844, G32774, D00060363, 28022, SIPSF-040018, 003500, 003600, 91.822.52.89, G17152, G32773, AQ-003500 and 21 more |
| Event type | Safety Notice |
| Date | May 3, 2019 |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 Matching device models 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