Finasteride Plus 1.25 mg Capsule recall: Contamination
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…
Why was Finasteride Plus 1.25 mg Capsule recalled?
Cross Contamination with Other Products; Finasteride Plus 1.25mg capsules were found to contain minoxidil.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #02-27-2020:04@11, Exp. August 25, 2020.
- Product
- 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…
- Recalling firm
- MasterPharm LLC
- Quantity
- 7260 capsules
- Distribution
- Nationwide in the U.S.
- Recall date
- May 20, 2020
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)