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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 90359

3 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
May 24, 2022
Product types
Drug
Classifications
Class I and Class II
Statuses
Completed
Recalling firm wording
Walmart Inc

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

3 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 3

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.

D-1157-2022
Recall number
D-1157-2022
Initiated
May 24, 2022
Classification
Class I
Status
Completed
Recalling firm
Walmart Inc
Quantity
1308 bottles total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot: LTARTKNGOMG30720, Exp Diciembre 2026

Distribution pattern

Nationwide in the USA.

drug · product 2 of 3

Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705.

D-1158-2022
Recall number
D-1158-2022
Initiated
May 24, 2022
Classification
Class II
Status
Completed
Recalling firm
Walmart Inc
Quantity
1308 bottles total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.

Code information

All product lots.

Distribution pattern

Nationwide in the USA.

drug · product 3 of 3

Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, a) 100-count bottles labeled with UPC 7 501031 111190 and UPC 6 09002 40885, and b) 2 pack of 100-count bottles per carton UPC 3 72426 01434

D-1159-2022
Recall number
D-1159-2022
Initiated
May 24, 2022
Classification
Class II
Status
Completed
Recalling firm
Walmart Inc
Quantity
1308 bottles total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.

Code information

All product lots.

Distribution pattern

Nationwide in the USA.