Allies Group recall: The One SPF 50 Invisible Sunscreen Gel
Allies Group Inc. is recalling The One SPF 50 Invisible Sunscreen Gel because of the wrong strength – 29,014 50mL Tubes; 27,492 3mL Sachets; 23,941, 20mL-Tube; 2,149 90mL-Tubes. The U.S. Food and Drug Administration published the recall on September 9, 2026; it began on August 14, 2026. Distributed nationwide.
Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
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| Product | The One SPF 50 Invisible Sunscreen Gel |
| Brand | Allies Group |
| Company | Allies Group Inc. |
| Type | Drugs |
| Classification | Class II |
| Recall date | August 14, 2026 |
| Published by FDA | September 9, 2026 |
| Quantity | 29,014 50mL Tubes; 27,492 3mL Sachets; 23,941, 20mL-Tube; 2,149 90mL-Tubes |
| Recall ID | 99652 |
Recalled products (4)
- THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 50ML - 1.7 fl. oz Tube, Made in U.S.A, Distributed by Allies Group Pte Ltd, Singapore 068914. UPC 8 885014 073224
- FDA recall number
- D-0823-2026
- Codes, lots and dates
- Lots: H22V01 Exp. 8/29/2026, H22V02 Exp. 8/30/2026, K22V02A Exp. 10/29/2026, M10V01 Exp. 01/21/2027, G23W02B Exp. 7/25/2027, G23W03 Exp. 8/4/2027, G23W03D Exp. 8/4/2027, K10W01A Exp. 10/17/2028, K10W01C Exp. 10/17/2028, M11W02 12/17/2028, F09X02 Exp. 6/17/2029.
- Quantity
- 29,014 50mL Tubes
- Classification
- Class II
- THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 3ml - 0.1 fl. oz, Sachet: Single use only, Made in the U.S.A, Distributed by Allies Group Pte Ltd, Singapore 068914.UPC 8 885014 073293
- FDA recall number
- D-0824-2026
- Codes, lots and dates
- Lots: C13W01A, Exp. 3/27/2027; G23W01A, Exp. 7/24/2027; M04W01, Exp. 12/10/2028.
- Quantity
- 27,492 3mL Sachets
- Classification
- Class II
- 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
- FDA recall number
- D-0825-2026
- Codes, lots and dates
- Lots: H22V02A, Exp. 8/30/2026; C13W01B, Exp. 3/27/2027; C24W01, Exp. 4/28/2027; G23W02, Exp. 7/25/2027; G23W01B, Exp. 7/24/2027; K10W02, Exp. 10/21/2028.
- Quantity
- 23,941, 20mL-Tube
- Classification
- Class II
- THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 90ml - 3 fl. oz. Tube, Made in the U.S.A, Distributed by Allies Group Pte Ltd, Singapore 068914. UPC 8 885014 075853
- FDA recall number
- D-0826-2026
- Codes, lots and dates
- Lots: G23W03B, Exp. 8/4/2027; A16X02, Exp. 1/20/2029: A16X03, Exp. 1/22/2029.
- Quantity
- 2,149 90mL-Tubes
- Classification
- Class II
Identifiers and details
- FDA event ID
- 99652
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Wilmington, DE, United States
Why it was recalled
The problem: the wrong strength.
The reason the FDA lists: “Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label.”
Where it was sold
Nationwide. Distribution as the FDA records it: “Nationwide within the U.S.A”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99652, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
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About this recall
Is Allies Group The One SPF 50 Invisible Sunscreen Gel recalled?
Yes. Allies Group Inc. recalled it on August 14, 2026; FDA published it September 9, 2026 (Class II). Only the lots, dates or models listed on this page are included.
Why was it recalled?
Because of the wrong strength. The reason given: Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label.
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
Nationwide.
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.