Karl Storz Endoscopy recalls Flexible Intubation Fiberscope, Model # 11301AB1
Recalled Product
Flexible Intubation Fiberscope, Model # 11301AB1
Hazard / Issue
The action is being initiated due to intubation scopes improperly manufactured with a double port luer instead of a single port luer.
Issued by
FDA
Affected States: VA, MO, CA, OH, NM, NY, CO, LA, ME
Lot/Code Info: Lot numbers: 2183827, 2195794, 2215741, 2229258, 2235373, 2248169, 2193769
View official government recall
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