MasterPharm LLC recalls
Every recall we track for MasterPharm LLC — 28 in all, all from 2020 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from MasterPharm LLC peaked in 2020 (28); 28 since 2017.
All FDA recall records for MasterPharm LLC since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 1 | 14 | 13 | 28 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for MasterPharm LLC recalls
What to do if you have a recalled MasterPharm LLC product
- Match the NDC and lot number on your bottle or box to the recall.
- Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
- Report side effects to FDA MedWatch.
All MasterPharm LLC recalls
3 shown- Use cautionDrug
MasterPharm LLC recalls Formula 82M (Minoxidil 5%/Tretinoin 0.01%/Fluocinolone acetonide 0.01%), a) 0.5 FL OZ (15 mL), b) 2 FL OZ (60 mL)
MasterPharm LLC recalls Formula 82M (Minoxidil/Tretinoin/Fluocinolone) bottles due to lack of processing controls. Check lot numbers and expiration dates.
MasterPharmJul 2, 2020 - UnratedDrug
MasterPharm LLC recalls Minoxidil/Biotin/Spironolactone 1.25/5/25 mg capsule, 90 capsules per bottle, This is a compounded drug not for resale,
MasterPharm recalls compounded minoxididil/biotin/spironolactone capsules due to elevated drug levels. This compounded drug (not for resale) may pose risks from high minoxidil content. Consumers should contact the manufacturer for details.
MasterPharmJun 9, 2020 - Lower riskDrug
MasterPharm LLC recalls Finasteride Plus 1.25 mg Capsule, a) 30-count bottle, b) 90-count bottle, Compounded Product Not for Resale,
MasterPharm recalls 30-count and 90-count Finasteride Plus 1.25mg capsules that contain minoxidil due to cross contamination. This may cause unintended side effects. Consumers should contact the manufacturer for details.
MasterPharmApr 14, 2020
MasterPharm LLC recall questions
How many recalls has MasterPharm LLC had?
28 recalls from MasterPharm LLC are on record with U.S. safety agencies, from 2020.
What is the most recent MasterPharm LLC recall?
MasterPharm LLC recalls Formula 82M (Minoxidil 5%/Tretinoin 0.01%/Fluocinolone acetonide 0.01%), a) 0.5 FL OZ (15 mL), b) 2 FL OZ (60 mL), dated Jul 2, 2020. Every MasterPharm LLC recall is listed on this page, newest first.
Why are MasterPharm LLC products recalled?
The most common reasons on record: Lack of Processing Controls (lack of assurance of conformity to specifications). (26).
What should I do if I have a recalled MasterPharm LLC product?
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
How do I get alerts for new MasterPharm LLC recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.