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Class II: temporary or reversible health riskTerminated

MasterPharm Yohimbine HCL 5 Recall

Yohimbine HCL 5

MasterPharm LLC · South Richmond Hill, NY

Risk level
Class II
Reported by FDA
Aug 5, 2020
Recall ID
D-1443-2020
Check your lot numberHow we source this data

Summary

MasterPharm recalled Yohimbine HCL 5 starting Jul 2, 2020. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1443-2020 on Aug 5, 2020. Reason: Lack of Processing Controls (lack of assurance of conformity to specifications). Status: Terminated.

Why it was recalled

Lack of Processing Controls (lack of assurance of conformity to specifications).

Product description

Yohimbine HCL 5.4mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600

Lot numbers, UPCs & expiration codes

01-20-2020:75@17, BUD 7/18/2020

Where it was sold

Nationwide in the U.S.

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-1443-2020
Classification
Class II
Status
Terminated
Recall initiated
Jul 2, 2020
FDA report date
Aug 5, 2020
Quantity
90 capsules
Recall type
Voluntary: Firm initiated
Recalling firm
MasterPharm LLC

Original FDA data

Every field from FDA enforcement report D-1443-2020, exactly as published.

Show all FDA fields
City
South Richmond Hill
State
NY
Status
Terminated
Country
United States
Event ID
85992
Address
11502 Liberty Ave Fl 2
Code information
01-20-2020:75@17, BUD 7/18/2020
Postal code
11419-1902
Report date
Aug 5, 2020
Product type
Drugs
Recall number
D-1443-2020
Classification
Class II
Recalling firm
MasterPharm LLC
Product quantity
90 capsules
Termination date
Feb 23, 2024
Reason for recall
Lack of Processing Controls (lack of assurance of conformity to specifications).
Voluntary / mandated
Voluntary: Firm initiated
Product description
Yohimbine HCL 5.4mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600
Distribution pattern
Nationwide in the U.S.
Recall initiation date
Jul 2, 2020
Initial firm notification
Letter
Center classification date
Jul 29, 2020

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1443-2020, published Aug 5, 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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