WOM Tube Set for lrrlgatlon — Class II medical device recall Z-2243-2024
Ongoing recall by WOM World Of Medicine AG, reported 2024-07-10, distributed nationwide. Incorrect transponder data was written on the RFID tags triggers the error message E03, Tube Set lnvalid, may
| Recall number | Z-2243-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | WOM World Of Medicine AG, Ludwigsstadt, N/A, Germany |
| Recall initiated | 2024-05-24 |
| Classified | 2024-07-01 |
| Reported by FDA | 2024-07-10 |
| Distributed | Nationwide (US) |
| Quantity | 1,700 units |
| UPC / GTIN / UDI-DI | 04056702003678 |
| Lot numbers | 4030902, 4030903 |
| Model numbers | T0449-01 |
Product
WOM Tube Set for lrrlgatlon, single-use- Intended to transport irrigation fluid to the patient in endoscopic surgeries. Distr. by Endoscopy Smith & Nephew Inc. REF Numbers: T0449-01
Reason for recall
Incorrect transponder data was written on the RFID tags triggers the error message E03, Tube Set lnvalid, may result in a delay of surgery
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-2243-2024. 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.