Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
WOM Tube Set for lrrlgatlon Recalled by WOM World Of Medicine AG Due to Incorrect transponder data was written on the RFID...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact WOM World Of Medicine AG directly.
Affected Products
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
Quantity: 1700 units
Why Was This Recalled?
Incorrect transponder data was written on the RFID tags triggers the error message E03, Tube Set lnvalid, may result in a delay of surgery
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About WOM World Of Medicine AG
WOM World Of Medicine AG has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report