# FDA recall D-0090-2019

> **Westlab Pharmacy, Inc. dba Westlab Pharmacy** · Class II · drug recall initiated 2018-08-10.

## Product

ADAA Cataract Drops, (Lido 1.47%, Phenyleph 0.294% Cyclopentolate 0.147%, Tropicamide 0.0735%, Moxiflox 0.0294%, Ketorolac 0.0147%) 1x 1cc syringe, Westlab Pharmacy, Inc., Gainesville, FL 32607 --- NDC 10002-2579-05

## Reason for recall

Lack of Process Controls

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0090-2019
- **Recalling firm:** Westlab Pharmacy, Inc. dba Westlab Pharmacy
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-08-10
- **Report date:** 2018-10-31
- **Termination date:** 2020-05-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Gainesville, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0090-2019

## Citation

> AI Analytics. FDA recall D-0090-2019. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/D-0090-2019. Source: US FDA. Licensed CC0.

---

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