VerifyRecall
Alerts
ACTIVE RECALL — CLASS IIActive recallD-0976-2022/FDA enforcement
Family Dollar Stores, LLC.·Cosmetics·May 17, 2022

Ambi Skincare Fade Cream Normal Skin, NET WT

What you need to know

Class II

  • What happened

    CGMP deviations: product stored outside of labeled temperature requirements.

  • 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 FDANationwide (US)More cosmetics

Advertisement

Ad

Know someone who bought this?

A quick share can keep a pantry check from becoming a missed warning.

Share via WhatsApp

Match before you discard

Product identification

Source: FDA COSMETICS

Brand nameFamily Dollar Stores, LLC.
Recalling firmFamily Dollar Stores, LLC.Chesapeake, VA, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • SKUs 2024222
Distribution area
Nationwide

USA Nationwide

United States

Quantity affectedNot provided by the FDA.
Recall initiationFDA report date: June 8, 2022
FDA recall numberD-0976-2022

Beyond the headline

The recall, in context

Family Dollar Stores, LLC. initiated this cosmetics recall on May 17, 2022. The FDA enforcement report states: CGMP deviations: product stored outside of labeled temperature requirements. The FDA report lists distribution as: USA Nationwide.

The FDA enforcement report describes the reason as: CGMP deviations: product stored outside of labeled temperature requirements.

Ambi Skincare Fade Cream Normal Skin, NET WT was made or distributed by Family Dollar Stores, LLC. in Chesapeake, VA, United States. This page reflects FDA report D-0976-2022, dated June 8, 2022.

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 Ambi Skincare Fade Cream Normal Skin, NET WT recall?

Family Dollar Stores, LLC. recalled Ambi Skincare Fade Cream Normal Skin, NET WT in an FDA Class II enforcement action reported as D-0976-2022. CGMP deviations: product stored outside of labeled temperature requirements.

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 Family Dollar Stores, LLC. 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-0976-2022. 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

Brand history

More recalls by Family Dollar Stores, LLC.

View brand
Class II·

Family Dollar Stores, LLC.

Banana Boat Sprt Clr Spry SPF50 6 FL OZ

CGMP Deviations: product held outside appropriate storage temperature conditions.

Nationwide (US)Cosmetics
Class II·

Family Dollar Stores, LLC.

Novelty Hand Sanitizer with Silicone Wrap

CGMP Deviations: product held outside appropriate storage temperature conditions.

Nationwide (US)Cosmetics

Related alerts

Recent cGMP deviations recalls

All alerts
Class II·

Shantou Qiwei Industrial Co., LTD

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

CGMP Deviations

CACosmetics
Class II·

Wellnov Supplements LLC

Liposomal Women's Liquid Multivitamin Drops with Iron

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

Nationwide (US) +1 countriesFood

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