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n.a.

Karl Storz GmbH & Co. KG · Model 24941F · UDI-DI 04048551083802

GCF Prescription
2
510(k) clearances
5
Adverse events
1
Recalls
10
Facilities

Description

Sealing cap with window

Recalls

DateFirmReason
2023-10-24Karl Storz EndoscopyThe efficacy of the manual cleaning process cannot be assured for the affected injection needles intended for general surgery and visceral surgery, which if used, may expose the pa

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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.