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n.a.
Karl Storz GmbH & Co. KG · Model 26206 · UDI-DI 04048551065044
KOH
Prescription
10
510(k) clearances
96
Adverse events
2
Recalls
83
Facilities
Description
Knife Holder
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-04-15 | Boston Scientific Corporation | Potential for pinholes (sterile barrier breach) on the edge of the pouch to potentially render the device non-sterile, and may result in a post-operative infection |
| 2003-02-20 | Portex, Inc | May have incorrectly printed graduation markings along the tube shaft. |
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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.