# FDA recall D-1488-2019

> **PharMEDium Services, LLC** · Class I · drug recall initiated 2019-06-07.

## Product

Hydromorphone HCl in 0.9% sodium chloride, 0.5mg per mL, 1 mL in 3mL BD  Syringe, PharMEDium 913 N Davis Ave Cleveland, MS 38732, 800-523-7749, NDC 61553-352-78

## Reason for recall

Incorrect Product Formulation; Firm's customer resource center (CRC) statement indicates that the product is sulfite free, however the product is produced with a raw material that contains sulfite

## Distribution

Nationwide within the United States

## Key facts

- **Recall number:** D-1488-2019
- **Recalling firm:** PharMEDium Services, LLC
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-06-07
- **Report date:** 2019-07-10
- **Termination date:** 2020-06-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Dayton, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1488-2019

## Citation

> AI Analytics. FDA recall D-1488-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-1488-2019. Source: US FDA. Licensed CC0.

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