# FDA recall Z-2243-2024

> **WOM World Of Medicine AG** · Class II · device recall initiated 2024-05-24.

## 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

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2243-2024
- **Recalling firm:** WOM World Of Medicine AG
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-05-24
- **Report date:** 2024-07-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Ludwigsstadt, N/A, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2243-2024

## Citation

> AI Analytics. FDA recall Z-2243-2024. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-2243-2024. Source: US FDA. Licensed CC0.

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