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ACTIVE RECALL — CLASS IIActive recallD-0854-2026/FDA enforcement
Shantou Qiwei Industrial Co., LTD·Cosmetics·Aug 8, 2026

Menow Sunscreen Pressed Powder SPF35 Pa+++, NET Content, 9g/0.32 OZ, Manufactured by: Shantzu…

What you need to know

Class II

  • What happened

    CGMP Deviations

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Current good manufacturing practice failures can affect product identity, strength, quality or purity.

  • Action required

    Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement.

Active recall · classified by the FDACAMore cosmetics

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Match before you discard

Product identification

Source: FDA COSMETICS

Brand nameShantou Qiwei Industrial Co., LTD
Recalling firmShantou Qiwei Industrial Co., LTDShantou, China
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot #: 2024/10/11, Exp. Date 10/10/2027
Distribution area
CA

CA only

United States

Quantity affected2970 units
Recall initiationFDA report date: September 30, 2026
FDA recall numberD-0854-2026

Beyond the headline

The recall, in context

Shantou Qiwei Industrial Co., LTD initiated this cosmetics recall on August 8, 2026. The FDA enforcement report states: CGMP Deviations. The FDA report lists distribution as: CA only.

The FDA enforcement report describes the reason as: CGMP Deviations

Menow Sunscreen Pressed Powder SPF35 Pa+++, NET Content, 9g/0.32 OZ, Manufactured by: Shantzu… was made or distributed by Shantou Qiwei Industrial Co., LTD in Shantou, China. This page reflects FDA report D-0854-2026, dated September 30, 2026.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, current good manufacturing practice failures can affect product identity, strength, quality or purity.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Set the product aside and do not apply it.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Menow Sunscreen Pressed Powder SPF35 Pa+++, NET Content, 9g/0.32 OZ, Manufactured by: Shantzu… recall?

Shantou Qiwei Industrial Co., LTD recalled Menow Sunscreen Pressed Powder SPF35 Pa+++, NET Content, 9g/0.32 OZ, Manufactured by: Shantzu… in an FDA Class II enforcement action reported as D-0854-2026. CGMP Deviations

What should I do if I bought this product?

Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Shantou Qiwei Industrial Co., LTD recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record D-0854-2026. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.