Flexible Intubation Fiberscope recall
Flexible Intubation Fiberscope, Model # 11301AB1
Why was Flexible Intubation Fiberscope recalled?
The action is being initiated due to intubation scopes improperly manufactured with a double port luer instead of a single port luer.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot numbers: 2183827, 2195794, 2215741, 2229258, 2235373, 2248169, 2193769
- Product
- Flexible Intubation Fiberscope, Model # 11301AB1
- Recalling firm
- Karl Storz Endoscopy
- Quantity
- 14 scopes
- Distribution
- US: VA, MO, CA, OH, NM, NY, CO, LA, ME, OUS: Canada
- Recall date
- September 11, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)