CLASS I Drug recall · Reported 27 Oct 2021 · FDA Enforcement Report

Coppertone Sport Mineral 50 Sunscreen Spray recalled by Beiersdorf

Beiersdorf is recalling Coppertone Sport Mineral 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, distributed nationwide in the US. The recall was initiated on 30 Sep 2021 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot# TN008KU, exp. date 03/31/2023 TN008KV, exp. date 03/31/2023
Quantity recalled142,236 cans

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0013-2022
FDA event ID
88770
Recalling firm
Beiersdorf, Wilton, CT
Classification
Class I
Status
Terminated
Recall initiated
30 Sep 2021
FDA classified
15 Oct 2021
Reported
27 Oct 2021
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Benzene

Timeline

30 Sep 2021Recall initiated by company
15 Oct 2021Classified by FDA+15 days
27 Oct 2021Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Chemical contamination; presence of benzene

Product as listed by the FDA

Coppertone SPORT MINERAL 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02870 1

Where it was distributed

Nationwide in the US

Nationwide

Questions about this recall

Why was it recalled?

Chemical contamination; presence of benzene

Which lots are affected?

Lot# TN008KU, exp. date 03/31/2023 TN008KV, exp. date 03/31/2023

Where was it sold?

Nationwide in the US

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

7 other products · FDA event 88770

More recalls from Beiersdorf

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