Key facts
| Recalling firm | Allies Group Inc. |
|---|---|
| Manufacturer | Not disclosed in the FDA record. |
| Brand name | Not disclosed in the FDA record. |
| Product description | THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 20ml - 0.7 fl. oz. Tube, Made in the U.S.A, Distributed by Allies Group Pte Ltd, Singapore 068914. UPC 8 885014 074733 |
| Classification | Class II |
| Recall number | D-0825-2026 |
| Report date | Not disclosed in the FDA record. |
| Status | Ongoing |
| Reason for recall | Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label. |
What consumers should do
Facilities, clinicians, and consumers holding an affected unit or lot of THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 20ml - 0.7 fl. oz. Tube, Made in the U.S.A, Distributed by Allies Group Pte Ltd, Singapore 068914. UPC 8 885014 074733 should stop using it for the purpose described in the recall notice and hold remaining stock pending instructions from Allies Group Inc.. FDA recall records typically direct the recalling firm to notify known accounts directly with a recall letter describing the specific corrective action -- replacement, field correction, refund, or return. Anyone who received the product through a distributor rather than directly from Allies Group Inc. should confirm with their supplier whether their specific lot or unit is on the affected list, since recall notices are lot- or unit-specific and not every unit of a product line is necessarily included. Questions about a specific unit's status should go to Allies Group Inc. directly or to the distributor that supplied it; Argus HQ is a public-record aggregator, not the recalling firm, and cannot confirm individual unit status.
What this classification means
A Class II recall is FDA’s middle classification. FDA assigns Class II when use of, or exposure to, the recalled product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote. FDA still requires the recalling firm to notify affected accounts and submit status reports on the correction, though the monitoring intensity is lower than for a Class I recall. FDA's Center for Devices and Radiological Health (for devices) or Center for Drug Evaluation and Research (for drugs) reviews the classification and can require additional corrective action if the initial response is judged insufficient. Because this record is filed as Class II, professionals and consumers handling an affected lot should treat FDA's own classification -- not this page's summary of it -- as the authoritative risk signal. A Class I recall is FDA’s most serious classification. FDA assigns Class I when there is a reasonable probability that use of, or exposure to, the recalled product will cause serious adverse health consequences or death. This classification does not mean harm has already occurred in every case -- it reflects FDA’s assessment of the realistic worst-case risk profile of the defect described in the recall, based on the reason for recall reported by the firm. Class I recalls receive the closest FDA monitoring of the three classes: the recalling firm typically must submit a recall strategy, periodic status reports, and effectiveness checks confirming that the affected lots have actually been removed from distribution or corrected in the field.
Allies Group Inc.’s FDA history
Argus HQ has recorded 4 total FDA actions tied to Allies Group Inc.: 0 warning letters, 4 recalls, 0 approval records, and 0 Form 483 inspection citations.
Frequently asked questions
- Why was THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homo recalled?
- FDA's recall record states the reason as: Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label.
- Who should I contact about this recall?
- Contact Allies Group Inc. directly, or the distributor/pharmacy that supplied the product, to confirm whether your specific lot or unit is affected. Argus HQ aggregates the public FDA recall record and is not the recalling firm.
- Has Allies Group Inc. had other FDA recalls or enforcement actions?
- Yes. Argus HQ has recorded 4 total FDA actions tied to Allies Group Inc., including 4 recalls and 0 warning letters.
- What is the FDA recall number for this event?
- FDA recall number D-0825-2026.
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Related enforcement actions
Full FDA history for Allies Group Inc.- Recall: Allies Group Inc. — Class II recall: THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocryle… →
- Recall: Allies Group Inc. — Class II recall: THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocryle… →
- Recall: Allies Group Inc. — Class II recall: THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocryle… →
Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder
Cite this record
Reusing this data in reporting or research? Here’s a ready-made citation.
Argus HQ Research (2026). FDA Recall Database: Class II Recall: THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone… by Allies Group Inc.. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/recall/allies-group-d-0825-2026-2026-09-09
"FDA Recall Database: Class II Recall: THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone… by Allies Group Inc.." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/recall/allies-group-d-0825-2026-2026-09-09.
Argus HQ Research. "FDA Recall Database: Class II Recall: THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone… by Allies Group Inc.." Digital Empire Holdings LLC. Accessed September 15, 2026. https://argushq.ai/recall/allies-group-d-0825-2026-2026-09-09.
@misc{argushq_argushq_ai_recall_allies_group_d_0825_2026_2026_09_09_2026,
title = {FDA Recall Database: Class II Recall: THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone… by Allies Group Inc.},
author = {{Argus HQ Research}},
year = {2026},
publisher = {Digital Empire Holdings LLC},
url = {https://argushq.ai/recall/allies-group-d-0825-2026-2026-09-09},
note = {Accessed: September 15, 2026}
}Source: FDA.gov — Recalls ↗

