Class II

Medical Device Recall: 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

WOM World Of Medicine AG · May 24, 2024

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.

States Affected

NATIONWIDE

Quantity Affected

1700 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2243-2024

Status: ongoing

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