WOM World of Medicine recalls Aquilex Fluid Control System Bag Deflector (REF AQL-100CBS) due to potential inaccurate fluid deficit readings during hysteroscopy procedures.
The deficit displayed by the pump can differ from the real deficit, leading potentially to patient risk.
WOM World of Medicine is recalling a specific component of their Aquilex Fluid Control System called the Bag Deflector (REF AQL-100CBS). This part can display a fluid deficit that differs from the actual amount, which may pose a risk to patients during hysteroscopy procedures.
The Bag Deflector may show a different fluid deficit level than what is actually present in the patient's body. This discrepancy could lead to incorrect medical decisions during hysteroscopy procedures, where fluid is used to distend the uterus.
Patients undergoing hysteroscopy procedures who use the recalled Bag Deflector component are at risk. Healthcare providers using this specific part in medical procedures are most affected.
Check for the product reference code AQL-100CBS on the Bag Deflector. The serial numbers listed in the recall include specific patterns starting with 1802CE through 1809CE.
Look for the serial numbers listed in the recall (e.g., 1802CE0558, 1803CE0226, etc.) on the Bag Deflector component.
The Bag Deflector may display a fluid deficit that differs from the actual amount, potentially leading to incorrect medical decisions during hysteroscopy procedures.
The product reference code is AQL-100CBS.
Check the serial number on the component against the list of numbers provided in the recall (e.g., 1802CE0558, 1803CE0226, etc.).
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-2767-2019 — WOM World of Medicine WOM World of Medicine Hello, I own a WOM World of Medicine that is covered by recall Z-2767-2019 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
