ACTIVE RECALL — CLASS IIActive recallD-0286-2026/FDA enforcement

Deodorant: a) Axe, Body Spray, Wild Spice, 6ct, 150ml

What you need to know

Class II
  • What happened

    CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.

  • 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

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Product identification

Source: FDA COSMETICS

Brand nameGold Star Distribution INC
Recalling firmGold Star Distribution INCMinneapolis, MN, United States
UPC / barcodes
6 00108 73646 98 08829 11166 88 08829 08910 30 48155 92109 2
Lot / date codes
  • All lots within expiry distributed by Gold Star Distribution.
Distribution area
Nationwide

US Nationwide.

United States

Quantity affectedNot provided by the FDA.
Recall initiationFDA report date: January 21, 2026
FDA recall numberD-0286-2026

Beyond the headline

The recall, in context

Gold Star Distribution INC initiated this cosmetics recall on December 26, 2025. The FDA enforcement report states: CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. The FDA report lists distribution as: US Nationwide.

The FDA enforcement report describes the reason as: CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.

Deodorant: a) Axe, Body Spray, Wild Spice, 6ct, 150ml was made or distributed by Gold Star Distribution INC in Minneapolis, MN, United States. This page reflects FDA report D-0286-2026, dated January 21, 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 UPC and lot code 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 Deodorant: a) Axe, Body Spray, Wild Spice, 6ct, 150ml recall?

Gold Star Distribution INC recalled Deodorant: a) Axe, Body Spray, Wild Spice, 6ct, 150ml in an FDA Class II enforcement action reported as D-0286-2026. CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.

What are the symptoms of Product safety recall exposure?

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.

Who is most at risk from Product safety recall?

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

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.

How do I get a refund from Gold Star Distribution INC?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall D-0286-2026 and keep the packaging, lot code and proof of purchase if you have them.

Is the Gold Star Distribution INC 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-0286-2026. 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

Brand history

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