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Class I: serious health riskTerminated

Human Science Foundation PRO ArthMax Dietary Supplement tablets Recall

PRO ArthMax Dietary Supplement tablets, 750 mg, 120 count bottles, Distributed by Human…

HUMAN SCIENCE FOUNDATION · Gardena, CA

Risk level
Class I
Reported by FDA
May 28, 2014
Recall ID
D-1327-2014
Check your lot numberHow we source this data

Summary

Human Science Foundation recalled PRO ArthMax Dietary Supplement tablets starting Jan 13, 2014. The FDA classified it as Class I (serious health risk) and published enforcement report D-1327-2014 on May 28, 2014. Reason: Marketed without an Approved NDA/ANDA; FDA analysis found the product to contain Chlorzoxazone, Nefopam, Diclofenac, Ibuprofen, Naproxen, and Indomethacin. Status: Terminated.

Why it was recalled

Marketed without an Approved NDA/ANDA; FDA analysis found the product to contain Chlorzoxazone, Nefopam, Diclofenac, Ibuprofen, Naproxen, and Indomethacin

Product description

PRO ArthMax Dietary Supplement tablets, 750 mg, 120 count bottles, Distributed by Human Science Foundation, Los Angeles, CA

Lot numbers, UPCs & expiration codes

Lot# 220113; Exp. 01/16 Lot# 800213; Exp. 03/16 Lot# U133000; Exp. 04/16 Lot# U143200; Exp. 08/16 Lot# YJK015311; Exp. 10/16

Where it was sold

Nationwide

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-1327-2014
Classification
Class I
Status
Terminated
Recall initiated
Jan 13, 2014
FDA report date
May 28, 2014
Quantity
24,268 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
HUMAN SCIENCE FOUNDATION

Original FDA data

Every field from FDA enforcement report D-1327-2014, exactly as published.

Show all FDA fields
City
Gardena
State
CA
Status
Terminated
Country
United States
Event ID
67265
Address
13722 Harvard Pl
Code information
Lot# 220113; Exp. 01/16 Lot# 800213; Exp. 03/16 Lot# U133000; Exp. 04/16 Lot# U143200; Exp. 08/16 Lot# YJK015311; Exp. 10/16
Postal code
90249-2527
Report date
May 28, 2014
Product type
Drugs
Recall number
D-1327-2014
Classification
Class I
Recalling firm
HUMAN SCIENCE FOUNDATION
Product quantity
24,268 bottles
Termination date
Sep 18, 2014
Reason for recall
Marketed without an Approved NDA/ANDA; FDA analysis found the product to contain Chlorzoxazone, Nefopam, Diclofenac, Ibuprofen, Naproxen, and Indomethacin
Voluntary / mandated
Voluntary: Firm initiated
Product description
PRO ArthMax Dietary Supplement tablets, 750 mg, 120 count bottles, Distributed by Human Science Foundation, Los Angeles, CA
Distribution pattern
Nationwide
Recall initiation date
Jan 13, 2014
Initial firm notification
Press Release
Center classification date
May 19, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1327-2014, published May 28, 2014. 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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