Fresenius Kabi USA, LLC recalls Fluphenazine Decanoate Injection, USP; 25 mg/mL, 5mL vials, Rx only, APP Pharmaceuticals, LLC Schaumburg, IL 60173, NDC…
- Recall date
- March 16, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0647-2017
- FDA classification
- Class III
- Brand / firm
- Fresenius Kabi USA, LLC
- Sold / distributed
- Nationwide within the US
Why it was recalled
Subpotent Drug
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Fluphenazine Decanoate Injection, USP; 25 mg/mL, 5mL vials, Rx only, APP Pharmaceuticals, LLC Schaumburg, IL 60173, NDC 63323-0272-05
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