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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 80473

1 recalled-product record grouped only because every row carries this exact official event ID.

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Event summary

Timeline bucket
July 05, 2018
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
The Hain Celestial Group, Inc. - Worldwide HQ

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 1

alba BOTANICA sport mineral sunscreen (titanium dioxide 7.0% and zinc oxide 9.0%), spf 45, 170 g (6 oz) tubes packaged in a) 4 tubes per case; b) 8 pack shipper display; Manufactured By: The Hain Celestial Group, Inc., Lake Success, NY 11042, UPC 7 24742 01102 4.

D-0920-2018
Recall number
D-0920-2018
Initiated
July 05, 2018
Classification
Class II
Status
Terminated
Quantity
47,128 tubes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Incorrect Product Formulation: wrong sunscreen product in the package.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Incorrect Product Formulation: wrong sunscreen product in the package.

Code information

Lot Codes: a) 7363B, 7363I, 8002C, 8002I, 8054J, 8055B, 8174A; and b) 7353

Distribution pattern

Nationwide in the USA

Field note

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