Finasteride Plus 1.25 mg Capsule
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Cross Contamination with Other Products; Finasteride Plus 1.25mg capsules were found to contain minoxidil.
Cause type: Cross-contamination
Traces of another drug - most often penicillin - got into the product from shared equipment or facilities. Even trace penicillin can trigger a severe allergic reaction in someone who was never meant to receive it. All cross-contamination recalls.
What was recalled
Finasteride Plus 1.25 mg Capsule, a) 30-count bottle, b) 90-count bottle, Compounded Product Not for Resale, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419.
Drug: Finasteride
- Recalling firm
- MasterPharm LLC
- Origin
- NY, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1269-2020 · FDA notice
Treat this as urgent. Class I means FDA judged there is a reasonable probability of serious harm. Find the lot number on your package; if it matches the recalled lots, do not take another dose before you have spoken to your pharmacist or prescriber - today, not next week. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.
Other Finasteride recalls
See allFinasteride Tablets
cGMP Deviations for the manufacturing Firm (Accord Healthcare) after their inspection.
Finasteride
cGMP deviations
Finasteride Tablets USP
CGMP Deviations: recalling drug products following an FDA inspection.
Finasteride Tablets USP 1 mg
CGMP Deviations: recalling drug products following an FDA inspection.
Other recalls by MasterPharm LLC
All 2020 recallsYohimbine HCL 5.4mg Capsule
Lack of Processing Controls (lack of assurance of conformity to specifications).
Vardenafil 20 mg Troche
Lack of Processing Controls (lack of assurance of conformity to specifications).
Testosterone/Anastrozole Pellet 100/6 mg
Lack of Processing Controls (lack of assurance of conformity to specifications).
Tadalafil 7 mg Capsule
Lack of Processing Controls (lack of assurance of conformity to specifications).
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