Southwest Technologies recalls Stimulen Collagen Moisturizing Lotion ST9555B due to dose audit failure after sterilization. Affected units include Lot 2104007 expiring 02/2024. Consumers should contact for details.
Dose audit failure after sterilization process
Southwest Technologies is recalling its Stimulen Collagen Moistur: Lotion ST9555B because of a dose audit failure after sterilization. This could affect product safety, though the specific risk isn't detailed in the recall notice.
The recall mentions a dose audit failure after the sterilization process. This could mean the product's safety checks weren't properly completed, potentially leading to unsafe dosing levels. However, the exact risk isn't specified in the notice.
Owners of the Stimulen Collagen Moisturizing Lotion ST9555B with lot number 2104007 (expiring 02/2024) are affected. People using this product are at risk if the dose audit failure impacts safety.
Check for the product name 'Stimulen Collagen Moisturizing Lotion' and model ST9555B. The affected lot number is 2104007, which expires on 02/2024.
Identify the lot number and expiration date on the product label to confirm if it's affected.
The recall states there was a dose audit failure after sterilization, but it doesn't specify if the product is unsafe. Consumers should check the product details to confirm.
The recall doesn't provide a remedy, so consumers should check the product details and contact Southwest Technologies for further instructions.
Look for the lot number 2104007 on the product label, which expires on 02/2024. If it matches, it's affected.
We’ve drafted a message you can send Southwest Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-2109-2021 — Southwest Technologies Southwest Technologies Hello, I own a Southwest Technologies that is covered by recall Z-2109-2021 from Southwest Technologies. 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.
