Karl Storz Endoscopy recalls Flexible Intubation Fiberscope, Model # 11301AB1
- Recall date
- April 24, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2447-2019
- FDA classification
- Class II
- Brand / firm
- Karl Storz Endoscopy
- Sold / distributed
- US: VA, MO, CA, OH, NM, NY, CO, LA, ME, OUS: Canada
Why it was recalled
The action is being initiated due to intubation scopes improperly manufactured with a double port luer instead of a single port luer.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Flexible Intubation Fiberscope, Model # 11301AB1
Get recall alerts
Free email alert whenever Karl Storz Endoscopy has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Karl Storz Endoscopy