Formula 82F recall
Formula 82F (Minoxidil 5%/Tretinoin 0.01%/Fluocinolone Acetonide 0.01%/Finasteride 0.25%), 0.5 FL OZ (15 mL) bottle MasterPharm, 115-02 Liberty Ave…
Why was Formula 82F recalled?
Lack of Processing Controls (lack of assurance of conformity to specifications).
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?
01-15-2020:70@3, 01-09-2020:48@2, BUD 7/7/2020 01-20-2020:79@11, 01-23-2020:55@11, BUD 7/18/2020 01-29-2020:18@1, 02-03-2020:89@8, BUD 7/26/2020
- Product
- Formula 82F (Minoxidil 5%/Tretinoin 0.01%/Fluocinolone Acetonide 0.01%/Finasteride 0.25%), 0.5 FL OZ (15 mL) bottle MasterPharm, 115-02 Liberty Ave…
- Recalling firm
- MasterPharm LLC
- Quantity
- 462 units
- Distribution
- Nationwide in the U.S.
- Recall date
- August 5, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)