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

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

WOM World Of Medicine AG 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 | SafeCheck