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Wellead Urethral Dilator

Well Lead Medical Co.,Ltd · Model U02A050110 · UDI-DI 06936881136498

KOE Prescription
10
510(k) clearances
222
Adverse events
3
Recalls
64
Facilities

Description

S Shape Urethral Dilator Set Hydrophilic 16-26Fr

Recalls

DateFirmReason
2019-01-04Cook Inc.The wire guide may be incorrectly loaded into the wire guide holder, leading to the stiff tip of the wire guide being introduced into the patient instead of the flexible tip.
2019-01-04Cook Inc.The wire guide may be incorrectly loaded into the wire guide holder, leading to the stiff tip of the wire guide being introduced into the patient instead of the flexible tip.
2005-08-01Cook Urological, Inc.Mislabeled as to size.

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Data 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.