Aesthetics Systems recalls Action De Gala and FuSion Conductive Gels due to potential bacterial contamination. These ultrasound gels may pose health risks if used without proper hygiene.
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021, FDA published a Letter to Health Care Providers to further address this issue: https://www.fda.gov/medical-devices/letters-health-care-providers/stop-using-all-eco-med-ultrasound-gels-and-lotions-due-risk-bacterial-contamination-letter-health.
Aesthetics Systems is recalling Action De Gala and FuSion Conductive Gels because they may contain bacterial contamination. Using these gels without proper hygiene could lead to health risks, especially in medical settings.
The gels may contain bacteria that can cause infections if not properly cleaned. This is particularly concerning in medical settings where hygiene is critical.
Healthcare providers and patients using ultrasound imaging equipment who have the gel with valid expiration dates. Those most at risk are individuals with compromised immune systems or open wounds.
Check for the product name 'Action De Gala' or 'FuSion Conductive Gel' with valid expiration dates. The gels are intended for ultrasound transducer use in medical imaging.
Verify the expiration date on the gel container to ensure it is valid.
Reach out to Aesthetics Systems for guidance on handling the gel if you have it.
The gels may contain bacterial contamination, which poses a health risk, especially in medical settings.
The official recall notice does not specify a deadline for action.
Look for the product names 'Action De Gala' or 'FuSion Conductive Gel' with valid expiration dates.
We’ve drafted a message you can send Aesthetics Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-0029-2022 — Aesthetics Systems Aesthetics Systems Hello, I own a Aesthetics Systems that is covered by recall Z-0029-2022 from Aesthetics Systems. 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.
