FDA Device recall Z-2425-2019
FLEXIBLE NEURO-FIBERSCOPE, 3.7MM X 34CM, Model # 11282BN1
- FDA Device
- Class II
- terminated
- Published 2019-09-04
On 2019-09-04 the FDA classified a Class II recall of FLEXIBLE NEURO-FIBERSCOPE, 3.7MM X 34CM, Model # 11282BN1 by Karl Storz Endoscopy, citing the action is being initiated due to Flexible Neuroscopes manufactured with the incorrect channel port.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2425-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-02-20 |
| Published | 2019-09-04 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Karl Storz Endoscopy |
| Distribution | AL, CA, FL, MA, MI, MO, NC, NH, OH, OR, PA, VA, WA |
Product
FLEXIBLE NEURO-FIBERSCOPE, 3.7MM X 34CM, Model # 11282BN1
Reason
The action is being initiated due to Flexible Neuroscopes manufactured with the incorrect channel port.
Identifiers
| code_info | SERIAL NUMBER: 2161516, 2204079, 2172240, 2198276, 2062041, 2178784, 2198341, 2220959, 2210200, 2183837, 2188370, 2247464, 2248783, 2194154, 2244117, 2039298 |
|---|
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-2425-2019%22
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