Electrode — Class II medical device recall Z-1308-2013
Terminated recall by Karl Storz Endoscopy America Inc, reported 2013-05-22, distributed nationwide. Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result
| Recall number | Z-1308-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Karl Storz Endoscopy America Inc, El Segundo, CA, United States |
| Recall initiated | 2009-06-01 |
| Classified | 2013-05-11 |
| Reported by FDA | 2013-05-22 |
| Terminated | 2013-05-13 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 9,432 units |
| Reason classes | sterility |
| Lot numbers | 36832 |
Product
Electrode, Coag, Ball End, 24FR (27050N/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).
Reason for recall
Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination.
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-1308-2013. 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.