FDAClass IIFebruary 5, 2020

Finasteride/Biotin 1 mg/50 mcg recall: Labeling Error

Finasteride/Biotin 1 mg/50 mcg

Why was Finasteride/Biotin 1 mg/50 mcg recalled?

Labeling: Incorrect or missing lot and/or expiration date. Products were compounded using expired components.

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: 60658:42 Use by: 12/28/2019

Product
Finasteride/Biotin 1 mg/50 mcg
Recalling firm
MPRX, Inc. dba Medical Park Pharmacy
Quantity
1 bottle
Distribution
TX
Recall date
February 5, 2020
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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