Flexible Intubation Fiberscope — Class II medical device recall Z-2447-2019
Terminated recall by Karl Storz Endoscopy, reported 2019-09-11, distributed in CA, CO, LA, ME, MO, NM, NY, OH…. The action is being initiated due to intubation scopes improperly manufactured with a double port luer instead
| Recall number | Z-2447-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Karl Storz Endoscopy, El Segundo, CA, United States |
| Recall initiated | 2019-04-24 |
| Classified | 2019-08-31 |
| Reported by FDA | 2019-09-11 |
| Terminated | 2020-12-04 |
| Distributed | CA, CO, LA, ME, MO, NM, NY, OH, VA |
| Countries outside the US | CA |
| Quantity | 14 scopes |
| Lot numbers | 2183827, 2193769, 2195794, 2215741, 2229258, 2235373, 2248169 |
| Model numbers | 11301AB1 |
Product
Flexible Intubation Fiberscope, Model # 11301AB1
Reason for recall
The action is being initiated due to intubation scopes improperly manufactured with a double port luer instead of a single port luer.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2447-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.