The Recall Desk
LowFDA (Drugs)·D-1107-2017·Announced 2017-08-23

Linde Eckstein SPF 10 Liquid Make-up Recalled for Subpotent Sun Protection

Linde Eckstein is recalling SPF 10 liquid make-up because the sun protection claim cannot be fully guaranteed. Consumers should stop using the product.

What this means for you

Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.

Our severity reasoning: The FDA classified this as a Class III recall, which by definition is unlikely to cause adverse health consequences. The hazard is a subpotent SPF claim, which is a minor labeling/efficacy issue rather than a direct safety threat like contamination or injury.

Plain-English summary

Linde Eckstein Gmbh + Co KG is recalling Make Up Perfect pastel (Titanium Dioxide) SPF 10 liquid make-up. The product is a 1 oz. (30 ml) bottle, Article 03310, manufactured in Germany. The recall involves specific lots: 210917 (Exp 09/21/2017) and 010918 (Exp 09/01/2018). The product was distributed throughout the United States.

The recall is issued because the product is labeled as having SPF 10 protection, but this claim cannot be 100% guaranteed. This is classified as a subpotent drug issue. The FDA has classified this recall as Class III, indicating that use of or exposure to the product is not likely to cause adverse health consequences.

Consumers who have this product should stop using it. The source text does not specify a return address or refund process, but the product should be discarded or returned according to local regulations or retailer policies.

The recalled product

Product
Make Up Perfect pastel (Titanium Dioxide) SPF 10 liquid make-up, 1 oz. Net Wt. 30 ml bottle, Art. 03310, Made in Germany, Doctor Eckstein, Linde Eckstein GMBH Co. Kg, 90522 Oberasbach, Germany, UPC 4 035219 033101.

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (4)

  • Lot #: 210917
  • Exp 09/21/2017
  • 010918
  • Exp 09/01/2018.

Distribution

Distribution scope not specified by the agency.

Part of a larger recall action

This product is one of 14 recalled by Linde Eckstein Gmbh + Co KG under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 14 products in this recall →