WOM World Of Medicine AG: Medical Device Recall in 2024 - (Recall #: Z-2243-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

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

Product Classification:

Class II

Date Initiated: May 24, 2024

Date Posted: July 10, 2024

Recall Number: Z-2243-2024

Event ID: 94749

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

Status: Ongoing

Product Quantity: 1700 units

Code Information:

UDI: 04056702003678 Lot Numbers: 4030902, 4030903

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated