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Class IIOngoing

MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++ recall

FDA recall D-0854-2026 · initiated Aug 8, 2026

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated Sep 30, 2026How we research

SHANTOU Qiwei industrial Co., Ltd recalled MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++ in Aug 2026 — an FDA Class II recall (D-0854-2026) because cGMP Deviations.

May cause temporary or medically reversible harm; low probability of serious harm.

Why it was recalled

cGMP Deviations

The manufacturing process itself

The FDA found the process itself out of compliance, usually before any defective product was identified.

This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.

Is your product affected? Check the lot number

A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.

Lot #: 2024/10/11, Exp. Date 10/10/2027

Quantity recalled: 2970 units

Details

Product
MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++, Net content, 9g/0.32 oz, Manufactured by: Shantzu Qiwei Industry Co. Ltd, Add: Quiwei Building, Yingloinguan, Xiashan, Chaonan district, Shantou City, Guangdong Province, China
Recalling company
SHANTOU Qiwei industrial Co., Ltd
Classification
Class II
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
CA only
Initiated
Aug 8, 2026
FDA report date
Sep 30, 2026
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++ recalled?
SHANTOU Qiwei industrial Co., Ltd recalled MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++ in Aug 2026 — an FDA Class II recall (D-0854-2026) because cGMP Deviations. May cause temporary or medically reversible harm; low probability of serious harm.
Why was MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++ recalled?
Per the FDA enforcement record, the reason for recall D-0854-2026 was: cGMP Deviations
Is a recalled MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++ dangerous to take?
An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
Which lots of MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++ are affected?
Distributed: CA only. The recall covers these lots — Lot #: 2024/10/11, Exp. Date 10/10/2027. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0854-2026.

Source: openFDA Drug Enforcement record D-0854-2026 ↗

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