Exact FDA event identifier

Event 96811

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

Event summary

Timeline bucket: March 29, 2025
Product types: Food
Classifications: Class II
Statuses: Terminated
Recalling firm wording: NRC Nutrition Pty Ltd

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

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

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

Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469

F-0930-2025

Recall number: F-0930-2025
Initiated: March 29, 2025
Classification: Class II
Status: Terminated
Recalling firm: NRC Nutrition Pty Ltd
Quantity: 7 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

inconsistent blending of iodine in the product

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

inconsistent blending of iodine in the product

Code information

Batch 42469

Distribution pattern

Texas, Minnesota, California, Indiana and Oklahoma