SHANTOU Qiwei industrial Co., Ltd recalls MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++, Net content, 9g/0.32 oz, Manufactured by: Shantzu Qiwei Industry Co. Ltd,
MENOW SPF35 pressed powder sunscreen with lot #2024/10/11 is recalled due to cGMP deviations. Consumers should check product details and contact the manufacturer for instructions.
Recall notice
cGMP Deviations
What happened, in plain English
MENOW SPF35 pressed powder sunscreen is being recalled because of manufacturing quality issues. This could affect product safety and may require action from consumers. Read more at govinfonow.com/recall/1287614-menow-spf35-sunscreen-powder-recall-cpg-deviations.
Source Summary by GovInfoNow · govinfonow.com/recall/1287614-menow-spf35-sunscreen-powder-recall-cpg-deviations · Published October 6, 2026 · Updated October 6, 2026 · FDA enforcement record: FDA #D-0854-2026
Cite this page
“MENOW SPF35 Sunscreen Powder Recall: CPG Deviations.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/1287614-menow-spf35-sunscreen-powder-recall-cpg-deviations. Based on FDA recall #D-0854-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0854-2026%22&limit=1).
Why it’s dangerous
The product was made under cGMP (current Good Manufacturing Practice) deviations, which means it may not meet safety standards. This could lead to potential safety issues with the sunscreen product.
Who’s affected
Owners of MENOW SPF35 pressed powder sunscreen with lot number 2024/10/11 are affected. People using this product in China are most at risk due to the manufacturing location.
How to tell if you have this one
Check for the product name 'MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++', net content 9g/0.32 oz, and lot number 2024/10/11. The product was manufactured in Shantou, China.
- Brand
MENOW- Category
Drug
What to do — step by step
Check Product Details
Look for the lot number 2024/10/11 on the product packaging.
Questions people ask
Is this product safe to use?
The recall is due to cGMP deviations, but the official notice does not specify if the product is safe to use.
How can I get a replacement?
The official recall notice does not mention replacement options.
Where was this product manufactured?
The product was manufactured in Shantou, China, by SHANTOU Qiwei industrial Co., Ltd.
Contact MENOW
We’ve drafted a message you can send MENOW to request your refund or repair — edit it as you like.
Subject: Recall D-0854-2026 — MENOW MENOW Hello, I own a MENOW that is covered by recall D-0854-2026 from MENOW. 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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Where this comes from
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 #D-0854-2026 (August 8, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0854-2026 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 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.