WOM World Of Medicine recalls single-use tube sets for endoscopic surgery due to RFID errors that may delay procedures. Affected units have specific reference numbers and lot codes.
Incorrect transponder data was written on the RFID tags triggers the error message E03, Tube Set lnvalid, may result in a delay of surgery
WOM World Of Medicine is recalling single-use tube sets used in endoscopic surgeries because faulty RFID tags can trigger an error message, potentially delaying surgery. This is a safety issue that requires immediate attention from medical staff using the product.
The tube set's RFID tags contain incorrect data that causes the system to display an error message (E03) when the device is scanned. This error can delay surgery by preventing the tube set from being properly recognized as valid.
Medical professionals using the WOM Tube Set for endoscopic procedures are most at risk. Patients undergoing surgery with this product may experience delays.
Check for reference numbers T0449-01 or UDI 04056702003678 on the tube set. Lot numbers 4030902 and 4030903 indicate affected units sold by Endoscopy Smith & Nephew Inc.
Verify the reference numbers and lot codes on the tube set to confirm if it is affected.
The RFID tags contain incorrect data that triggers an error message (E03), potentially delaying surgery.
Check the reference numbers and lot codes to see if it is affected; no specific action is required if it is not listed.
The recall record does not mention a remedy or fix.
We’ve drafted a message you can send WOM World Of Medicine to request your refund or repair — edit it as you like.
Subject: Recall Z-2243-2024 — WOM World Of Medicine WOM World Of Medicine Hello, I own a WOM World Of Medicine that is covered by recall Z-2243-2024 from WOM World Of Medicine. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
