# FDA recall D-0813-2018

> **Milbar Laboratories, Inc.** · Class II · drug recall initiated 2018-05-04.

## Product

Naturmetic SPF 50 Sunscreen (Octinoxate 7.5%, Zinc Oxide 10.5%), 2.0 fl oz/60mL bottles, Fortis BioPharma, Magnolia, TX 77354.

## Reason for recall

GMP Deviations

## Distribution

Within the United States and Puerto Rico

## Key facts

- **Recall number:** D-0813-2018
- **Recalling firm:** Milbar Laboratories, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-05-04
- **Report date:** 2018-05-23
- **Termination date:** 2019-06-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** East Haven, CT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0813-2018

## Citation

> AI Analytics. FDA recall D-0813-2018. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-0813-2018. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
