KARL STORZ SE & CO KG
1 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (1)
Registered facilities (11)
- KARL STORZ SE & CO KG FEI 3014342096 · DE
- KARL STORZ ENDOSCOPY-AMERICA, INC. FEI 2020550 · MA
- KARL STORZ ENDOVISION, INC. FEI 1221826 · MA
- STORZ ENDOSKOP PRODUKTIONS GMBH FEI 3002808273 · CH
- Karl Storz Endoscopy-America, Inc. FEI 3007475226 · CA
- KARL STORZ IMAGING, INC. FEI 2027009 · CA
- KARL STORZ SE & CO. KG FEI 3002808268 · DE
- KARL STORZ SE & CO. KG FEI 3010707607 · DE
- KARL STORZ SE & CO. KG FEI 3006546082 · DE
- KARL STORZ VIDEO ENDOSCOPY ESTONIA OUE FEI 3004644065 · EE
- KARL STORZ Endovision, Inc. FEI 3032429484 · MA
Recalls & enforcement
- Class IITerminated2016-02-29Endoscope cleaning brush 11276CL may not fit resulting in an inability to insert the brush in to the channel of the intended endoscope or to completely pass it through such channel.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “KARL STORZ SE & CO KG — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-8010119-karl-storz-se-co-kg/
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