Solar Defense Sheer Sunscreen Broad Spectrum SPF50 — Class II drug recall D-0812-2018
Terminated recall by Milbar Laboratories, Inc., reported 2018-05-23, distributed in PR. GMP Deviations
| Recall number | D-0812-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Milbar Laboratories, Inc., East Haven, CT, United States |
| Recall initiated | 2018-05-04 |
| Classified | 2018-05-15 |
| Reported by FDA | 2018-05-23 |
| Terminated | 2019-06-26 |
| Distributed | PR |
| Quantity | 2,156 tubes |
| Reason classes | cgmp |
| Lot numbers | KU455-2, KU455-6 |
| Expiration dates | 2020-11-09, 2020-11-26 |
Product
Solar Defense Sheer Sunscreen Broad Spectrum SPF50 (Octinoxate 7.5%, Zinc Oxide 10.5%), 2.5 FL OZ. 74 mL, Distributed by: BeautyRx LLC, NY, NY 10128
Reason for recall
GMP Deviations
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0812-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.