Use caution Medical device recall · FDA · Published July 17, 2023

WOM World Of Medicine recalls Aquilex Fluid Control System: Display may freeze causing

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.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2629-2023Medical device WOM World Of Medicine ›

Use caution until it’s fixed

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

Take action

Contact the company

Recalling firmWOM World Of Medicine AGAlte Poststr. 11 · Ludwigsstadt, Germany

✎ GovInfoNow plain-language explainer

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. Read more at govinfonow.com/recall/57643-wom-world-of-medicine-recalls-aquilex-fluid-control-system-display.

Source Summary by GovInfoNow · govinfonow.com/recall/57643-wom-world-of-medicine-recalls-aquilex-fluid-control-system-display · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2629-2023

Cite this page

“WOM World Of Medicine recalls Aquilex Fluid Control System: Display may freeze causing.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/57643-wom-world-of-medicine-recalls-aquilex-fluid-control-system-display. Based on FDA recall #Z-2629-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2629-2023%22&limit=1).

WOM World Of Medicine AG is recalling the Aquilex Fluid Control System due to a potential fluid overload hazard, according to the FDA. The Food and Drug Administration announced the Class II recall on July 17, 2023.

How to tell if you have it

Brand: WOM World Of Medicine
Product: Aquilex Fluid Control System
Models: AQL-100PBS, AQL-100P
UDI-DI: 04056702006914
Serial Numbers: US S1802CE0538 through 2303CE0661; Canada 1802CE0650 through 2104CE0706
Units affected: 1287

The hazard

The display of inflow volume can reach its limit of 30,000 ml during long procedures 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.

Context

GovInfoNow's records show WOM World Of Medicine AG has 4 other recalls on record since 2018-10-22. Other recent recalls of similar products include Baxter Novum IQ Syringe Pump Recall (2026-08-11), Philips AneurysmFlow Software Recall (2026-03-19) and Fresenius Medical Care 2008T BlueStar Hemodialysis Machine Recall (2026-06-30).

How to tell if you have this one

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.

Brand
WOM World Of Medicine
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Model
Identify if your device is model AQL-100PBS or AQL-100P with the listed serial numbers.
Contact Manufacturer
Contact WOM World Of Medicine for specific instructions on how to address the issue.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

FDA distribution: “Nationwide Foreign: Canada, Australia, New Zealand, Belgium, France, Germany, Ireland, Netherlands, Spain, Sweden, Norway, Switzerland, UK, Kuwait, Qatar, Turkey, UAE” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 3 months after the firm started it.

Jul 17, 2023Firm started the recall
Sep 22, 2023FDA classified it Class II
Oct 4, 2023Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/57643-wom-world-of-medicine-recalls-aquilex-fluid-control-system-display">WOM World Of Medicine recalls Aquilex Fluid Control System: Display may freeze causing (GovInfoNow)</a>

Where this comes from

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.

Official source: FDA Recall #Z-2629-2023 (July 17, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2629-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.