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RECALL RECORD — CLASS IIRecall closedD-1670-2012/FDA enforcement
Island Kinetics Dba Covalence·Cosmetics·Jul 13, 2012

Cosmedix Serious Protection, Natural SPF 28 Sunscreen, 3.3 Fl.oz/100ml (100 g), Distributed By…

What you need to know

Class II

  • What happened

    Microbial Contamination of Non Sterile Product; mold

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. The product may not deliver the sun protection stated on its label, increasing the risk of sunburn and UV exposure.

  • 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.

Recall closed · classified by the FDADistribution not listedMore cosmetics

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Match before you discard

Product identification

Source: FDA COSMETICS

Brand nameIsland Kinetics Dba Covalence
Recalling firmIsland Kinetics Dba CovalenceChandler, AZ, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Batch # P030911C, Exp 03/13
  • Batch # P022811A, Exp 02/13.
Distribution area

Atlanta, Georgia

United States

Quantity affected5311 bottles
Recall initiationFDA report date: September 5, 2012
FDA recall numberD-1670-2012

Beyond the headline

The recall, in context

Island Kinetics Dba Covalence initiated this cosmetics recall on July 13, 2012. The FDA enforcement report states: Microbial Contamination of Non Sterile Product; mold. The FDA report lists distribution as: Atlanta, Georgia.

The FDA enforcement report describes the reason as: Microbial Contamination of Non Sterile Product; mold

Cosmedix Serious Protection, Natural SPF 28 Sunscreen, 3.3 Fl.oz/100ml (100 g), Distributed By… was made or distributed by Island Kinetics Dba Covalence in Chandler, AZ, United States. This page reflects FDA report D-1670-2012, dated September 5, 2012.

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, visible or laboratory-detected mold can signal a moisture, temperature or seal failure.

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

Mold contamination

Symptoms to watch for

Eating a moldy product may cause nausea, vomiting, diarrhea or allergic reactions. Do not intentionally inspect, smell or taste a suspect product.

Higher-risk groups

People with mold allergies, asthma, a weakened immune system, pregnant people and young children should be especially cautious.

What to do now

  1. 1Stop using or eating the affected product and keep it away from children and pets.
  2. 2Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer.
  3. 3If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

Visible mold can indicate a moisture, packaging or temperature failure.

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 Cosmedix Serious Protection, Natural SPF 28 Sunscreen, 3.3 Fl.oz/100ml (100 g), Distributed By… recall?

Island Kinetics Dba Covalence recalled Cosmedix Serious Protection, Natural SPF 28 Sunscreen, 3.3 Fl.oz/100ml (100 g), Distributed By… in an FDA Class II enforcement action reported as D-1670-2012. Microbial Contamination of Non Sterile Product; mold

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 affected product and keep it away from children and pets. Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer. If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

Is the Island Kinetics Dba Covalence recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record D-1670-2012. 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.