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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 87759

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

Open FDA event record

Event summary

Timeline bucket
July 13, 2020
Product types
Food
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Lopez Gonzalez Santana Corporation

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

2 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 2

BTREX PLUS, Dietary Supplement 2 Caplets, UPC 05380930802 (Physician Samples)

F-0540-2021
Recall number
F-0540-2021
Initiated
July 13, 2020
Classification
Class III
Status
Terminated
Quantity
lots #32179  1405 and Lot #33278 - 0.

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviations: Presence of damaged tablets

Code information

Lot# 32179, Exp. 9/2022 Lot# 33278, Exp. 12/2022

Distribution pattern

Domestic distribution only-PR

food · product 2 of 2

BTREX PLUS, Dietary Supplement 100 Caplets

F-0541-2021
Recall number
F-0541-2021
Initiated
July 13, 2020
Classification
Class III
Status
Terminated
Quantity
662 bottles.

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviations: Presence of damaged tablets

Code information

Lot # 33491, Exp. 12/22

Distribution pattern

Domestic distribution only-PR