RECALL RECORD — CLASS IIIRecall closedD-1098-2017/FDA enforcement

Beautipharm Body Moisturizing Balm SPF 10 (Octocrylene 4% and Octyl Methoxycinnamide 4%) Body…

What you need to know

Class III
  • What happened

    Subpotent Drug: products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. 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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Product identification

Source: FDA COSMETICS

Brand nameLinde Eckstein Gmbh + Co kg
Recalling firmLinde Eckstein Gmbh + Co kgOberasbach, Germany
UPC / barcodes
4 035219 03150 3
Lot / date codes
  • Lot #: 201017, Exp 10/20/17
  • 290618, Exp 06/29/18
  • 040419, Exp 04/04/19.
Distribution area

Distributed throughout the United States

United States

Quantity affected105 creams
Recall initiationFDA report date: August 23, 2017
FDA recall numberD-1098-2017

Beyond the headline

The recall, in context

Linde Eckstein Gmbh + Co kg initiated this cosmetics recall on July 17, 2017. The FDA enforcement report states: Subpotent Drug: products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed. The FDA report lists distribution as: Distributed throughout the United States.

The FDA enforcement report describes the reason as: Subpotent Drug: products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed.

Beautipharm Body Moisturizing Balm SPF 10 (Octocrylene 4% and Octyl Methoxycinnamide 4%) Body… was made or distributed by Linde Eckstein Gmbh + Co kg in Oberasbach, Germany. This page reflects FDA report D-1098-2017, dated August 23, 2017.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, the product may not deliver the sun protection stated on its label, increasing the risk of sunburn and UV exposure.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

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 Beautipharm Body Moisturizing Balm SPF 10 (Octocrylene 4% and Octyl Methoxycinnamide 4%) Body… recall?

Linde Eckstein Gmbh + Co kg recalled Beautipharm Body Moisturizing Balm SPF 10 (Octocrylene 4% and Octyl Methoxycinnamide 4%) Body… in an FDA Class III enforcement action reported as D-1098-2017. Subpotent Drug: products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed.

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 Linde Eckstein Gmbh + Co kg 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-1098-2017. 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.