SA3 recalls Silatrix Oral Gel 10% due to microbial testing failure. Affected units may contain harmful bacteria. Consumers should contact SA3 for details.
Due to failure of microbial testing for total aerobic microbial count (TAMC).
SA3 is recalling Silatrix Oral Gel 10% because microbial testing failed, potentially allowing harmful bacteria to grow. This could cause health issues if used without proper testing.
The gel failed microbial testing for total aerobic microbial count, meaning harmful bacteria could grow in the product. This poses a risk of infection or other health problems if the gel is ingested.
People who use Silatrix Oral Gel 10% for medical purposes are affected. Those with compromised immune systems may be at higher risk.
Check for Product Number 69420-8351-1 and Lot Number U701SF1 on the packaging. The gel is sold under the brand name Silatrix Oral Gel 10%.
Reach out to SA3 directly for specific instructions on how to handle the recalled product.
The recall indicates microbial testing failed, so the product may contain harmful bacteria. Do not use until SA3 provides instructions.
Look for Product Number 69420-8351-1 and Lot Number U701SF1 on the packaging.
Contact SA3 for specific instructions on how to handle the recalled product.
We’ve drafted a message you can send SA3 to request your refund or repair — edit it as you like.
Subject: Recall Z-0856-2022 — SA3 SA3 Hello, I own a SA3 that is covered by recall Z-0856-2022 from SA3. 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.
