Kroger Specialty Pharmacy, Inc. recalls Sutent 37.5 mg capsules x28 NDC 00069-0830-38 28 days supply
- Recall date
- April 3, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0787-2018
- FDA classification
- Class II
- Brand / firm
- Kroger Specialty Pharmacy, Inc.
- Sold / distributed
- MS, LA, AR, IL, FL
Why it was recalled
Lack of Processing Controls.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Sutent 37.5 mg capsules x28 NDC 00069-0830-38 28 days supply
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