CLASS III Food recall · Reported 26 May 2021 · FDA Enforcement Report

Btrex Plus, Dietary Supplement 2 Caplets recalled

Lopez Gonzalez Santana is recalling Btrex Plus, Dietary Supplement 2 Caplets, distributed in Puerto Rico. The recall was initiated on 13 Jul 2020 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot# 32179, Exp. 9/2022 Lot# 33278, Exp. 12/2022
Quantity recalledlots #32179  1405 and Lot #33278 - 0.

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0540-2021
FDA event ID
87759
Recalling firm
Lopez Gonzalez Santana, Rio Piedras, PR
Classification
Class III
Status
Terminated
Recall initiated
13 Jul 2020
FDA classified
19 May 2021
Reported
26 May 2021
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Product category
Dietary Supplements

Timeline

13 Jul 2020Recall initiated by company
19 May 2021Classified by FDA+310 days
26 May 2021Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

CGMP Deviations: Presence of damaged tablets

Product as listed by the FDA

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

Where it was distributed

Domestic distribution only-PR

Puerto Rico

Questions about this recall

Why was it recalled?

CGMP Deviations: Presence of damaged tablets

Which lots are affected?

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

Where was it sold?

Domestic distribution only-PR

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 87759

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