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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 65128

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
May 01, 2013
Product types
Food
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Atlantic Pro Nutrients, Inc. dba XYMOGEN

Dossier provenance

Source snapshots represented here

  • openFDA Food 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

1 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.

food · product 1 of 1

XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and 180 capsule bottles

F-1523-2013
Recall number
F-1523-2013
Initiated
May 01, 2013
Classification
Class I
Status
Terminated
Quantity
16,268 units

App-derived interpretation

Undeclared allergen reason.undeclared_allergen · v1.0.0
Undeclared Soy and Milk

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Undeclared Soy and Milk on the label.

Code information

All SKUs

Distribution pattern

AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NM, NY, OH, OK, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY, District of Columbia and Hawaii

Field note

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