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Saffron
Coloplast A/S · Model 520340 · UDI-DI 05708932757423
PBQ
Prescription
1
510(k) clearances
66
Adverse events
1
Recalls
9
Facilities
Description
Fixation Tool
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-12-13 | FEMSelect Ltd | Certain lots may not have been packaged wth the Channel Tube Limiter. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.