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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 94118

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

Open FDA event record

Event summary

Timeline bucket
February 23, 2024
Product types
Food
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Backstage Center DBA CTC Seller

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

Alipotec Raiz de Tejocote dietary supplements, Net. Wt. 0.35oz, plastic bottle labeled with the "Alipotec King" sticker. Store at room temperature.

F-1147-2024
Recall number
F-1147-2024
Initiated
February 23, 2024
Classification
Class I
Status
Terminated
Quantity
280 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of tejocote.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of tejocote.

Code information

Lot Codes: 238124 Expiration date:08-2027

Distribution pattern

Products are distributed to 250 consignees; all consignees were direct to consumer purchases. Distributed nationwide.