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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 89996

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

Open FDA event record

Event summary

Timeline bucket
March 24, 2022
Product types
Food
Classifications
Class II
Statuses
Terminated
Recalling firm wording
The Procter & Gamble Company

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

Align Digestive De-Stress Capsules 21ct bottle packaged in paper carton 12 cartons per case

F-1012-2022
Recall number
F-1012-2022
Initiated
March 24, 2022
Classification
Class II
Status
Terminated
Quantity
23,928 cartons

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product failed micro testing. Firm sent product for destruction, but was redirected for sale through online store.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Product failed micro testing. Firm sent product for destruction, but was redirected for sale through online store.

Code information

Lot No. 1022171991 Product No. 80347747 Best By Date: 07/31/2022

Distribution pattern

Product was sent to a 3rd party for destruction due to not meeting micro specs