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.
“Southwest Technologies Stimulen Lotion Recall: Dose Audit Failure Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62459-southwest-technologies-stimulen-lotion-recall-dose-audit-failure-risk. Based on FDA recall #Z-2109-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2109-2021%22&limit=1).
The FDA announced on May 28, 2021, that Southwest Technologies Inc. is recalling Stimulen Collagen Moisturizing Lotion due to a dose audit failure after sterilization. The voluntary Class II recall affects 2,016 units distributed in Malaysia.
How to tell if you have it
Brand: Southwest Technologies
Product: Stimulen Collagen Moisturizing Lotion
Model/Part Number: ST9555B
Lot Code: 2104007
Expiration Date: 02/2024
The hazard
The recall is due to a dose audit failure after the sterilization process. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show Southwest Technologies Inc has issued two other recalls since December 28, 2017. On November 18, 2019, the company recalled Elasto-Gel Wound Dressings due to mold contamination risk. Other recent recalls of similar products include Medical Action Industries Epidural Kits Recall (July 23, 2026), Medline Convenience Kits Recall (January 7, 2026), and Medline Syringes Recall (February 25, 2026).
How to tell if you have this one
Check for the product name 'Stimulen Collagen Moisturizing Lotion' and model ST9555B. The affected lot number is 2104007, which expires on 02/2024.
Brand
Southwest Technologies
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Details
Identify the lot number and expiration date on the product label to confirm if it's affected.
How this recall unfolded
Recall timeline
FDA published this recall 2 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-2109-2021 (May 28, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2109-2021 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.