Karl Storz SE & CO — Class II medical device recall Z-1474-2024
Ongoing recall by Karl Storz Endoscopy, reported 2024-04-10, distributed nationwide. Inadequate reprocessing validation evidence
| Recall number | Z-1474-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Karl Storz Endoscopy, El Segundo, CA, United States |
| Recall initiated | 2024-02-27 |
| Classified | 2024-04-03 |
| Reported by FDA | 2024-04-10 |
| Distributed | Nationwide (US) |
| Quantity | 147 units |
| UPC / GTIN / UDI-DI | 04048551193587 |
| Model numbers | 723014 |
Product
Karl Storz SE & CO. KG, REF 723014, Uvula Retractor, For Veterinary Use Only, Rx Only
Reason for recall
Inadequate reprocessing validation evidence
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-1474-2024. 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.