Decision published on June 19, 2026 halts sale, distribution, and use of products while the manufacturer conducts voluntary recall
A health decision involving dietary supplements raised an alert among Brazilian consumers this Friday, June 19, 2026.
The National Health Surveillance Agency (Anvisa) suspended the commercialization, distribution, and use of 11 batches of IDNLABS supplements.
The determination affects products of creatine, BCAA, beta-alanine, multivitamins, and multiminerals.
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The manufacturer announced the start of the voluntary recall of the batches included in the decision.
The measure was formalized by Resolution-RE nº 2.149/2026, published in the Official Gazette of the Union.

Inspection found flaws in the supplements
Quality tests identified quantities of ingredients below the values stated on the packaging, according to data released by Anvisa.
The inspection found consumption recommendations exceeding the limits authorized by health regulations.
Problems in the designation of the supplements and in the presentation of mandatory information were also recorded.
Some labels presented unauthorized claims for the dietary supplements category.
The consumption recommendation for beta-alanine was not in accordance with the conditions permitted by legislation.
The irregularities led to the cancellation of the sanitary notifications of the products.

Creatine had three batches suspended
Three batches of creatine powder dietary supplement were included in Anvisa’s decision:
- 0147.05.2025
- 0148.05.2025
- 0285.05.2025
Products with these identifications cannot be marketed, distributed, or used while the suspension remains in effect.
BCAA entered the list of affected products
The determination also reached three batches of BCAA 2-1-1 in tablets:
- 003.01.2025
- 004.01.2025
- 044.01.2025
The sale and use of these batches remain halted until a new decision by the health authority.
Beta-alanine showed irregular recommendation
Three batches of beta-alanine powder were also included in the resolution:
- 0267.08.2025
- 0149.05.2025
- 079.02.2025
Anvisa reported that the product’s usage recommendation was outside the authorized conditions.
Multivitamins were also suspended
Two batches of multivitamins and multiminerals in coated tablets were included in the measure:
- 005.01.2026
- 0211.07.2025
The inspection identified the absence of mandatory warnings and difficulties in viewing the information on the labels.
These issues contributed to the cancellation of the supplements’ notifications.
What should the consumer do?
Consumers who have supplements from IDNLABS should check the batch number printed on the packaging.
Use should be discontinued when the identification matches any of the suspended batches.
The consumer should contact the manufacturer to receive guidance on the recall.
The prohibition will remain valid until a new decision by Anvisa.
IDNLABS had not yet presented a position
The report sought IDNLABS to request clarifications about the suspended batches and the measures taken.
The company had not yet presented a position by the time this article was closed.
The information was disclosed by the National Health Surveillance Agency and the Official Gazette of the Union.
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