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Class I: serious health riskCompleted

Walmart Artri King Reforzado con Ortiga Omega 3 Recall

Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, 100-count bottles, Melchor O…

Walmart Inc · Bentonville, AR

Risk level
Class I
Reported by FDA
Jun 22, 2022
Recall ID
D-1157-2022
Check your lot numberHow we source this data

Summary

Walmart recalled Artri King Reforzado con Ortiga Omega 3 starting May 24, 2022. The FDA classified it as Class I (serious health risk) and published enforcement report D-1157-2022 on Jun 22, 2022. Reason: Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted with undeclared diclofenac, an FDA approved nonsteroidal anti-inflammatory drug (NSAID) for the treatment of pain and inflammation. Status: Completed.

Why it was recalled

Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted with undeclared diclofenac, an FDA approved nonsteroidal anti-inflammatory drug (NSAID) for the treatment of pain and inflammation.

Product description

Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, 100-count bottles, Melchor Ocampo No. 55 Local D, Delegacion Xochimilco, C.P. 16800, Mexico, D.F., UPC 7 501031 111190.

Lot numbers, UPCs & expiration codes

Lot: LTARTKNGOMG30720, Exp Diciembre 2026

Where it was sold

Nationwide in the USA.

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-1157-2022
Classification
Class I
Status
Completed
Recall initiated
May 24, 2022
FDA report date
Jun 22, 2022
Quantity
1308 bottles total
Recall type
Voluntary: Firm initiated
Recalling firm
Walmart Inc

Original FDA data

Every field from FDA enforcement report D-1157-2022, exactly as published.

Show all FDA fields
City
Bentonville
State
AR
Status
Completed
Country
United States
Event ID
90359
Address
702 Sw 8th St Ms 275
Code information
Lot: LTARTKNGOMG30720, Exp Diciembre 2026
Postal code
72716-6299
Report date
Jun 22, 2022
Product type
Drugs
Recall number
D-1157-2022
Classification
Class I
Recalling firm
Walmart Inc
Product quantity
1308 bottles total
Reason for recall
Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted with undeclared diclofenac, an FDA approved nonsteroidal anti-inflammatory drug (NSAID) for the treatment of pain and inflammation.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, 100-count bottles, Melchor Ocampo No. 55 Local D, Delegacion Xochimilco, C.P. 16800, Mexico, D.F., UPC 7 501031 111190.
Distribution pattern
Nationwide in the USA.
Recall initiation date
May 24, 2022
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Jun 24, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1157-2022, published Jun 22, 2022. 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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