FDA Device recall Z-1309-2013
Electrode, Roller Ball, 24FR (27050NK/6)
- FDA Device
- Class II
- terminated
- Published 2013-05-22
On 2013-05-22 the FDA classified a Class II recall of Electrode, Roller Ball, 24FR (27050NK/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-1309-2013 |
| 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, Roller Ball, 24FR (27050NK/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 36833 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Other recalls by Karl Storz Endoscopy America
- Broncho Flexible Fiberscope, models: 11001BN1, 11002BD1, 11004BC1, and 11009BC1. " Examination and treatment of the tracheobronchial tree C…
FDA Device · Class II · 2013-12-25 · Karl Storz Endoscopy America - Intubation Flexible Fiberscope, Models: 11301AA1, 11301BN1, 11302BD1, 11302BD2, 11304BC1, 11340BC1, 11301BND1, 11302BDD1, and 11302BDD2. "…
FDA Device · Class II · 2013-12-25 · Karl Storz Endoscopy America - Axillent Debakey Grasping Forceps, Part No. 33821DYD In general the surgeons use 33821DYD Debakey forceps to grasp tissue
FDA Device · Class II · 2013-12-18 · Karl Storz Endoscopy America - 27023WU Balloon Catheter, 3 Fr., 2/pkg, sterile, contains latex
FDA Device · Class II · 2013-07-24 · Karl Storz Endoscopy America - Knife, Cold, Straight (27068K/6)
FDA Device · Class II · 2013-05-22 · Karl Storz Endoscopy America
All Karl Storz Endoscopy America recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1309-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.