FDAApril 24, 2019device
Flexible Intubation Fiberscope, Model # 11301AB1
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The action is being initiated due to intubation scopes improperly manufactured with a double port luer instead of a single port luer.
What to do
FDA enforcement status: Terminated
Brands named
karl storz endoscopykarlkarl storz
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDATangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1) TNG4002-IND. (2) TNG-4007-6pk.2026-03-23
- FDAKARL STORZ - ENDOSKOPE, REF: 27002L, Uretero-Renoscope, 9.5 Fr., 6¿, 43 cm, NON STERILE, RxONLY, CE 01232024-12-19
- FDAKARL STORZ - ENDOSKOPE, REF: 27003L, MICHEL Uretero-Renoscope, 9.5 Fr., 43cm, RxONLY, CE01232024-12-19
- FDAKARL STORZ - ENDOSKOPE, REF: 27011K, Ureteroscope, 8 Fr., 6¿, 34cm, CE 01232024-12-19
- FDAKARL STORZ - ENDOSKOPE, REF: 27000L,Uretero-Renoscope, 7 Fr., 6¿, 43 cm, NON STERILE, RxONLY, CE 01232024-12-19
- FDAKARL STORZ - ENDOSKOPE, REF: 27002KP, Pediatric Uretero-Renoscope 7.3 Fr., NON STERILE, CE 01232024-12-19
- FDAKARL STORZ - ENDOSKOPE, REF: 27030KA, Cysto-Urethroscope, NON STERILE, CE2024-12-19
- FDAKARL STORZ - ENDOSKOPE, REF: 27001L, Uretero-Renoscope, 8 Fr., 6¿, 43 cm, NON STERILE, RxONLY, CE 01232024-12-19
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