Vertra Elemental Resistance — Class II drug recall D-0100-2018
Terminated recall by EAI-JR286 INC, reported 2017-12-06, distributed nationwide. CGMP Deviations: products manufactured in a manner that may impact product quality that includes but is not li
| Recall number | D-0100-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | EAI-JR286 INC, Torrance, CA, United States |
| Recall initiated | 2017-11-28 |
| Classified | 2017-11-30 |
| Reported by FDA | 2017-12-06 |
| Terminated | 2019-08-09 |
| Distributed | Nationwide (US) |
| Quantity | 5,355 tubes |
| Reason classes | cgmp |
| UPC / GTIN / UDI-DI | 00894140001030 |
| Lot numbers | 03/18, 511103, 609124 |
Product
Vertra Elemental Resistance (Octyl Methoxycinnamate 6%, Oxybenzone 5%, Titanium Dioxide 6.3%, Zinc Oxide 9.9%) Sun Protection Cream, SPF 50+, Net. Wt. 2.8 oz (80 g) tube in a carton, Distributed by Vertra/EAI-JR286, 20100 S Vermont Ave, Torrance, CA 90502, Made In Australia, UPC 8 94140 00103 0.
Reason for recall
CGMP Deviations: products manufactured in a manner that may impact product quality that includes but is not limited to failed viscosity.
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-0100-2018. 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.