Testosterone Cypionate + Progesterone, 200 mg/ 2.5 mg/mL ,10 mL amber glass vials, Rx Only, Compounded by AXIA Pharmaceutical, Los Angeles, CA 90025
Reported: August 9, 2017 Initiated: July 12, 2017 #D-1040-2017
Product Description
Testosterone Cypionate + Progesterone, 200 mg/ 2.5 mg/mL ,10 mL amber glass vials, Rx Only, Compounded by AXIA Pharmaceutical, Los Angeles, CA 90025
Reason for Recall
CGMP Deviations
Details
- Recalling Firm
- Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical
- Units Affected
- 120 vials
- Distribution
- There were only one customer in California
- Location
- Los Angeles, CA
Frequently Asked Questions
What product was recalled? ▼
Testosterone Cypionate + Progesterone, 200 mg/ 2.5 mg/mL ,10 mL amber glass vials, Rx Only, Compounded by AXIA Pharmaceutical, Los Angeles, CA 90025. Recalled by Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical. Units affected: 120 vials.
Why was this product recalled? ▼
CGMP Deviations
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 9, 2017. Severity: Moderate. Recall number: D-1040-2017.
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