FDA Device recall Z-2447-2019
Flexible Intubation Fiberscope, Model # 11301AB1
- FDA Device
- Class II
- terminated
- Published 2019-09-11
On 2019-09-11 the FDA classified a Class II recall of Flexible Intubation Fiberscope, Model # 11301AB1 by Karl Storz Endoscopy, citing the action is being initiated due to intubation scopes improperly manufactured with a double port luer instead of a single port luer.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2447-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-04-24 |
| Published | 2019-09-11 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Karl Storz Endoscopy |
| Distribution | CA, CO, LA, ME, MO, NM, NY, OH, VA |
Product
Flexible Intubation Fiberscope, Model # 11301AB1
Reason
The action is being initiated due to intubation scopes improperly manufactured with a double port luer instead of a single port luer.
Identifiers
| code_info | Lot numbers: 2183827, 2195794, 2215741, 2229258, 2235373, 2248169, 2193769 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2447-2019%22
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