International safety notice
Urgent Field Safety Notice for Kwart Retro-Inject Ureteral Stent Set / Salle Intraoperative Pyeloplasty Stent Set by Cook Incorporated
Germany / BfArM · DEU · May 8, 2019
Key facts
| Title | Urgent Field Safety Notice for Kwart Retro-Inject Ureteral Stent Set / Salle Intraoperative Pyeloplasty Stent Set by Cook Incorporated |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Kwart Retro-Inject Ureteral Stent Set / Salle Intraoperative Pyeloplasty Stent Set |
| Manufacturer | Cook Incorporated |
| Models | G17151, AQ-003600, G14844, D00060363, AQ-003700, G14837, F14-00B, 334440, 003500, G18168, SIPSF-040018-59, F14-00A and 16 more |
| Date | May 8, 2019 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No 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