Bioventus recalls EXOGEN Ultrasound Coupling Gel with potential microbial particulates. Affected units include specific part numbers and lots. Consumers should check their product details and contact Bioventus for guidance.
Product may contain white particulates that are microbial in nature.
Bioventus is recalling EXOGEN Ultrasound Coupling Gel due to possible microbial particulates. This could pose a health risk if the gel is used in medical procedures. Affected products have specific part numbers and production lots.
The gel may contain white particulates that are microbial in nature. If these particles enter the body during medical procedures, they could cause infections or other health issues. However, the risk is not immediate and depends on proper use and handling.
Medical professionals using the EXOGEN Ultrasound Coupling Gel for diagnostic imaging are most at risk. Patients receiving procedures with this gel may also be affected if the product is contaminated.
Check the product label for part numbers: 71034475, 71034694, 71034695, or 81079892. Also look for specific lots listed in the recall notice, such as 190235 or 200207.
Review the product label for part numbers and lots to confirm if your EXOGEN Ultrasound Coupling Gel is affected.
The recall states the gel may contain microbial particulates, but it is not immediately unsafe. Affected units should be checked and handled with caution.
Check the product label for part numbers: 71034475, 71034694, 71034695, or 81079892, and specific lots like 190235 or 200207.
Contact Bioventus directly for guidance on next steps, as the recall does not specify a remedy.
We’ve drafted a message you can send Bioventus to request your refund or repair — edit it as you like.
Subject: Recall Z-0810-2021 — Bioventus Bioventus Hello, I own a Bioventus that is covered by recall Z-0810-2021 from Bioventus. 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.
