FDAFDA · Food and drugs·Recall number Z-2243-2024
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
Published July 10, 2024 · Recall initiated: May 24, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Incorrect transponder data was written on the RFID tags triggers the error message E03, Tube Set lnvalid, may result in a delay of surgery
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- WOM World Of Medicine AG
- Distributor
- US Nationwide distribution.
- Lot
- UDI: 04056702003678 Lot Numbers: 4030902, 4030903
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- Germany
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