Reported Sep 11, 2019 · Terminated
Flexible Intubation Fiberscope, Model # 11301AB1
Karl Storz Endoscopy
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Karl Storz Endoscopy · 2151 E Grand Ave · El Segundo, CA · 90245-5017
Is this the product you have?
- Flexible Intubation Fiberscope, Model # 11301AB1
- Lot codes and dates
- Lot numbers
2183827219579422157412229258223537322481692193769
- Lot numbers
- Amount recalled
- 14 scopes
Where it was sold
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.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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