WOM World Of Medicine recalls Aquilex Fluid Control System models AQL-100PBS and AQL-100P with serial numbers starting 1802CE... due to display freezing at 30,000 ml causing potential fluid overload during procedures.
The display of inflow volume can reach its limit of 30,000 ml during long procdeure and the inflow volume display will freeze at the maximum value while the deficit will start counting backwards until 0 ml is reached and may result in fluid overload
WOM World Of Medicine is recalling Aquilex Fluid Control System devices (models AQL-100PBS and AQL-100P) because the inflow volume display can freeze at 30,000 ml during long procedures, potentially causing fluid overload. This risk occurs when the display shows the maximum value and the deficit counter starts counting backward to zero.
During long procedures, the inflow volume display can reach its limit of 30,000 ml and freeze at that maximum value. This causes the deficit counter to start counting backward from 30,000 ml to 0 ml, which may lead to fluid overload in the patient.
Healthcare professionals using the Aquilex Fluid Control System during hysteroscopy procedures are most at risk. Patients undergoing diagnostic or operative hysteroscopy with these devices may experience fluid overload.
Check for models AQL-100PBS and AQL-100P with serial numbers starting with 1802CE, 1803CE, 1804CE, 1805CE, 1806CE, 1807CE, 1808CE, 1809CE, 1811CE, 1902CE, 1903CE, 1904CE, 1906CE, 1908CE, 1911CE, 1912CE, 2002CE, 2006CE, 2008CE, 2102CE, 2103CE, 2104CE, 2105CE, 2106CE, 2107CE, 2108CE, 2109CE, 2201CE, 2204CE, 2205CE, 2206CE, 2209CE, 2210CE, 2211CE, 2212CE, 2301CE, 2302CE, 2303CE.
Identify if your device is model AQL-100PBS or AQL-100P with the listed serial numbers.
Contact WOM World Of Medicine for specific instructions on how to address the issue.
The display may freeze at 30,000 ml during long procedures, causing the deficit counter to count backward to zero, which can lead to fluid overload in the patient.
Check for models AQL-100PBS or AQL-100P with serial numbers starting with 1802CE, 1803CE, 1804CE, 1805CE, 1806CE, 1807CE, 1808CE, 1809CE, 1811CE, 1902CE, 1903CE, 1904CE, 1906CE, 1908CE, 1911CE, 1912CE, 2002CE, 2006CE, 2008CE, 2102CE, 2103CE, 2104CE, 2105CE, 2106CE, 2107CE, 2108CE, 2109CE, 2201CE, 2204CE, 2205CE, 2206CE, 2209CE, 2210CE, 2211CE, 2212CE, 2301CE, 2302CE, or 2303CE.
The recall does not specify a fix or remedy; contact WOM World Of Medicine for specific instructions.
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-2629-2023 — WOM World Of Medicine WOM World Of Medicine Hello, I own a WOM World Of Medicine that is covered by recall Z-2629-2023 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.
