# FDA recall D-1251-2019

> **Advanced Pharma Inc.** · Class II · drug recall initiated 2019-04-26.

## Product

HYDROmorphone 20 mg/100 mL Injectable Solution, Hydromorphone HCl 20 mg 0.9% Sodium Chloride 100 mL, Sterile single use bag, Compounded Drug, Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404, NDC: 42852-221-10

## Reason for recall

Sub-potency

## Distribution

Nationwide in the US

## Key facts

- **Recall number:** D-1251-2019
- **Recalling firm:** Advanced Pharma Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-04-26
- **Report date:** 2019-05-08
- **Termination date:** 2019-10-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Houston, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1251-2019

## Citation

> AI Analytics. FDA recall D-1251-2019. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/D-1251-2019. Source: US FDA. Licensed CC0.

---

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