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CODMAN

Cerenovus, Inc. · Model 83-1325 · UDI-DI 20886704042737

GYK Prescription
1
510(k) clearances
15
Adverse events
1
Recalls
21
Facilities

Description

CODMAN Peel-Away Catheter Introducer 12.5 FR.

Recalls

DateFirmReason
2010-12-22Integra LifeSciences Corp.Peritoneal Introducer Sheaths were incorrectly labeled as 61 cm instead of 46 cm.

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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.