Fluphenazine Decanoate Injection, USP; 25 mg/mL, 5mL vials, Rx only, APP Pharmaceuticals, LLC Schaumburg, IL 60173, NDC 63323-0272-05
Reported: April 12, 2017 Initiated: March 16, 2017 #D-0647-2017
Product Description
Fluphenazine Decanoate Injection, USP; 25 mg/mL, 5mL vials, Rx only, APP Pharmaceuticals, LLC Schaumburg, IL 60173, NDC 63323-0272-05
Reason for Recall
Subpotent Drug
Details
- Recalling Firm
- Fresenius Kabi USA, LLC
- Units Affected
- 118,224 vials
- Distribution
- Nationwide within the US
- Location
- Lake Zurich, IL
Frequently Asked Questions
What product was recalled? ▼
Fluphenazine Decanoate Injection, USP; 25 mg/mL, 5mL vials, Rx only, APP Pharmaceuticals, LLC Schaumburg, IL 60173, NDC 63323-0272-05. Recalled by Fresenius Kabi USA, LLC. Units affected: 118,224 vials.
Why was this product recalled? ▼
Subpotent Drug
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 12, 2017. Severity: Low. Recall number: D-0647-2017.
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