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Class I: serious health riskTerminated

MasterPharm Minoxidil/Biotin/Spironolactone 1 Recall

Minoxidil/Biotin/Spironolactone 1

MasterPharm LLC · South Richmond Hill, NY

Risk level
Class I
Reported by FDA
Jul 8, 2020
Recall ID
D-1363-2020
Check your lot numberHow we source this data

Summary

MasterPharm recalled Minoxidil/Biotin/Spironolactone 1 starting Jun 9, 2020. The FDA classified it as Class I (serious health risk) and published enforcement report D-1363-2020 on Jul 8, 2020. Reason: Super-potent Drug: This recall has been initiated due to the elevated presence of minoxidil and biotin. Status: Terminated.

Why it was recalled

Super-potent Drug: This recall has been initiated due to the elevated presence of minoxidil and biotin.

Product description

Minoxidil/Biotin/Spironolactone 1.25/5/25 mg capsule, 90 capsules per bottle, This is a compounded drug not for resale, Store at room temperature, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419.

Lot numbers, UPCs & expiration codes

Lot #: 01-09-2020:13@8, Exp. 7/7/2020

Where it was sold

FL and MD

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-1363-2020
Classification
Class I
Status
Terminated
Recall initiated
Jun 9, 2020
FDA report date
Jul 8, 2020
Quantity
300 capsules
Recall type
Voluntary: Firm initiated
Recalling firm
MasterPharm LLC

Original FDA data

Every field from FDA enforcement report D-1363-2020, exactly as published.

Show all FDA fields
City
South Richmond Hill
State
NY
Status
Terminated
Country
United States
Event ID
85839
Address
11502 Liberty Ave Fl 2
Code information
Lot #: 01-09-2020:13@8, Exp. 7/7/2020
Postal code
11419-1902
Report date
Jul 8, 2020
Product type
Drugs
Recall number
D-1363-2020
Classification
Class I
Recalling firm
MasterPharm LLC
Product quantity
300 capsules
Termination date
Oct 16, 2023
Reason for recall
Super-potent Drug: This recall has been initiated due to the elevated presence of minoxidil and biotin.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Minoxidil/Biotin/Spironolactone 1.25/5/25 mg capsule, 90 capsules per bottle, This is a compounded drug not for resale, Store at room temperature, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419.
Distribution pattern
FL and MD
Recall initiation date
Jun 9, 2020
Initial firm notification
Letter
Center classification date
Jun 26, 2020

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1363-2020, published Jul 8, 2020. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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