# FDA recall D-0484-2015

> **RemedyRepack Inc.** · Class II · drug recall initiated 2015-02-18.

## Product

KETOROLAC TROM 30 MG/ML INJ, 1 mL glass vials  repackaged individually inside an amber glass bottle, packaged by RemedyRepack, Indiana, PA, mfg by Hospira, Inc. Lake Forest, IL NDC 61786-0055-01

## Reason for recall

Crystallization

## Distribution

PA, OK.

## Key facts

- **Recall number:** D-0484-2015
- **Recalling firm:** RemedyRepack Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-02-18
- **Report date:** 2015-04-15
- **Termination date:** 2015-08-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Indiana, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0484-2015

## Citation

> AI Analytics. FDA recall D-0484-2015. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-0484-2015. Source: US FDA. Licensed CC0.

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