Home / Recalls / Medical Devices
Karl Storz Endoscopy recalls Flexible Intubation Fiberscope, Model # 11301AB1
Recalled September 11, 2019 · FDA recall Z-2447-2019 · Karl Storz Endoscopy
Hazard
The action is being initiated due to intubation scopes improperly manufactured with a double port luer instead of a single port luer. · FDA Class II
Units
14 scopes
Sold at
US: VA, MO, CA, OH, NM, NY, CO, LA, ME, OUS: Canada
Description
The action is being initiated due to intubation scopes improperly manufactured with a double port luer instead of a single port luer.
Product
Flexible Intubation Fiberscope, Model # 11301AB1
Manufacturer(s)
Karl Storz Endoscopy
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →