# FDA recall D-0997-2019

> **Avella of Deer Valley, Inc. Store 38** · Class II · drug recall initiated 2019-02-08.

## Product

Labetalol 20mg, HCL, USP Injectable Solution, 20mg/4mL (5 mg per mL), 4mL single use syringe. Repackaged by Avella Specialty Pharmacy 24416 N 19th Avenue, Phoenix, AZ 85085 (877) 794-0404, NDC 42852-822-71.

## Reason for recall

Labeling: Incorrect or Missing Lot and/or Exp Date:The product labels contain a Two-Dimensional ( 2D ) barcode that, when scanned, reveals information specific to the batch of the labeled product, including Expiration Date.  The expiration date included within these 2D barcodes is incorrect and does not match the correct expiration date listed on the face of the label itself.

## Distribution

Distribution to 13 states: Alabama, Arizona, California, Colorado, Florida, Idaho, Michigan, Minnesota, North Carolina, New Jersey, Oregon, Pennsylvania, Texas.

## Key facts

- **Recall number:** D-0997-2019
- **Recalling firm:** Avella of Deer Valley, Inc. Store 38
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-02-08
- **Report date:** 2019-02-20
- **Termination date:** 2020-02-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Phoenix, AZ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0997-2019

## Citation

> AI Analytics. FDA recall D-0997-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0997-2019. Source: US FDA. Licensed CC0.

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