RemedyRepack Inc. recalls KETOROLAC TROM 30 MG/ML INJ, 1 mL glass vials repackaged individually inside an amber glass bottle, packaged by RemedyR…
- Recall date
- April 23, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0974-2015
- FDA classification
- Class II
- Brand / firm
- RemedyRepack Inc.
- Sold / distributed
- PA and OK
Why it was recalled
Crystallization
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
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
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