FindMyRecallSubscribe
Class II: temporary or reversible health riskTerminated

API Solutions Azelaic Acid 99 Recall

Azelaic Acid 99

API Solutions Inc. · Daphne, AL

Risk level
Class II
Reported by FDA
Aug 4, 2021
Recall ID
D-0696-2021
Check your lot numberHow we source this data

Summary

API Solutions recalled Azelaic Acid 99 starting Jul 15, 2021. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0696-2021 on Aug 4, 2021. Reason: cGMP Deviations. Status: Terminated.

Why it was recalled

cGMP Deviations

Product description

Azelaic Acid 99.0+% Micro 500 Grams, Distributed By: A.P.I. Solutions Daphne Alabama Manufactured by: Yicheng Chemicals Corp. China Distributed by: Syntec Pharma Corp New York

Lot numbers, UPCs & expiration codes

Lot #: AZA181105, Exp 11/09/2021

Where it was sold

AL, AZ, CO, FL, VA

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-0696-2021
Classification
Class II
Status
Terminated
Recall initiated
Jul 15, 2021
FDA report date
Aug 4, 2021
Quantity
1 bottle
Recall type
Voluntary: Firm initiated
Recalling firm
API Solutions Inc.

Original FDA data

Every field from FDA enforcement report D-0696-2021, exactly as published.

Show all FDA fields
City
Daphne
State
AL
Status
Terminated
Country
United States
Event ID
88289
Address
25309 Friendship Rd
Code information
Lot #: AZA181105, Exp 11/09/2021
Postal code
36526-6278
Report date
Aug 4, 2021
Product type
Drugs
Recall number
D-0696-2021
Classification
Class II
Recalling firm
API Solutions Inc.
Product quantity
1 bottle
Termination date
Feb 8, 2022
Reason for recall
cGMP Deviations
Voluntary / mandated
Voluntary: Firm initiated
Product description
Azelaic Acid 99.0+% Micro 500 Grams, Distributed By: A.P.I. Solutions Daphne Alabama Manufactured by: Yicheng Chemicals Corp. China Distributed by: Syntec Pharma Corp New York
Distribution pattern
AL, AZ, CO, FL, VA
Recall initiation date
Jul 15, 2021
Initial firm notification
Letter
Center classification date
Jul 28, 2021

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0696-2021, published Aug 4, 2021. 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.

How we source and update recall data · Report incorrect information

Other recent drug recalls