# FDA recall D-0496-2019

> **Advanced Pharma Inc.** · Class II · drug recall initiated 2019-02-06.

## Product

Fentanyl in 0.9% Sodium Chloride QS 0.5 mL, 5 mcg/0.5 mL with up to 0.1 mL of overfill Injectable Solution, Sterile single use syringe, Rx only, Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404, NDC 42852-210-72

## Reason for recall

Labeling: Incorrect expiration date.

## Distribution

PA

## Key facts

- **Recall number:** D-0496-2019
- **Recalling firm:** Advanced Pharma Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-02-06
- **Report date:** 2019-02-27
- **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-0496-2019

## Citation

> AI Analytics. FDA recall D-0496-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0496-2019. Source: US FDA. Licensed CC0.

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