WOM World Of Medicine AG: Device Recall
Recall #Z-2243-2024 · 05/24/2024
Class II: Risk
Recall Details
- Recall Number
- Z-2243-2024
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- WOM World Of Medicine AG
- Status
- Ongoing
- Date Initiated
- 05/24/2024
- Location
- Ludwigsstadt, N/A, Germany
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1700 units
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
Product Description
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
Distribution Pattern
US Nationwide distribution.
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.