FDA Device recall Z-1310-2013
Electrode, Barrel Bar, 24FR (27050NX/6)
- FDA Device
- Class II
- terminated
- Published 2013-05-22
On 2013-05-22 the FDA classified a Class II recall of Electrode, Barrel Bar, 24FR (27050NX/6) by Karl Storz Endoscopy America, citing possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1310-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2009-06-01 |
| Published | 2013-05-22 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Karl Storz Endoscopy America |
| Distribution | US |
Product
Electrode, Barrel Bar, 24FR (27050NX/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).
Reason
Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination.
Identifiers
| code_info | Lot 36850 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1310-2013%22
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