Disclosure: A number of the links on this page are affiliate links. The editors may earn a commission when you buy through these links. This costs you nothing extra.
TRE House publishes its certificates at its lab reports page. The four July 1, 2026 gummy certificates were issued by ACS Laboratory; TRE House describes its testing laboratories as ISO 17025-certified, and each certificate says ACS Laboratory is accredited to ISO/IEC 17025:2017. For the four listed July batches, the certificates report both 4-AcO-DET and 4-AcO-DMT as <LOQ.
What do the July 2026 TRE House gummy lab reports say?
The certificates identify an Extra Strength Mushroom Gummies flavor, its TRE House batch number, the sampled product and the July 1, 2026 completion date. In the synthetic-tryptamine panel, each reports <LOQ for 4-AcO-DET and 4-AcO-DMT. That means the lab did not report a quantified result at or above its stated limit of quantitation for either compound in that sample.
| Flavor | TRE House batch | Completion date | 4-AcO-DET | 4-AcO-DMT |
|---|---|---|---|---|
| Strawberry Dream certificate | THMG-SD128 | July 1, 2026 | <LOQ | <LOQ |
| Blue Raspberry certificate | THMG-BR128 | July 1, 2026 | <LOQ | <LOQ |
| Watermelon Wonder certificate | THMG-WW128 | July 1, 2026 | <LOQ | <LOQ |
| Sour Tropical certificate | THMG-ST128 | July 1, 2026 | <LOQ | <LOQ |
These are batch-specific reports. Match the batch printed on your bag to the batch at the top of the certificate before treating it as the report for your product.
How do you read a TRE House certificate?
Use the Strawberry Dream certificate for batch THMG-SD128 as a practical example. It identifies the client as TRE House, the product as Extra Strength Mushroom Gummies – Strawberry Dream, the sample as mushroom edibles for ingestion, the TRE House batch date as June 1, 2026, sampling date as June 9, 2026, and completion date as July 1, 2026.
- Batch number: This is the key matching field. Flavor alone is not enough because one flavor can have more than one report over time.
- Sampling and completion dates: These tell you when the laboratory received or sampled the material and when it completed the report.
- Sample versus product: The certificate says its results relate only to the material or product analyzed. It is a report on that submitted sample, not a substitute for matching the printed batch on your own package.
- Panels: The July certificates list amanita analytes, psilocybe mushroom analytes, synthetic tryptamines, pathogenic microbiology, heavy metals, mycotoxins, pesticides and residual solvents.
The summary on each July certificate marks pathogenic microbiology, heavy metals, mycotoxins and residual solvents as passed, and the pesticide section of each certificate is marked passed. Their amanita panel lists ibotenic acid, muscarine and muscimol; each is reported <LOQ. Their psilocybe panel lists psilocybin, psilocin and other named analytes; each listed result is <LOQ.
What do LOD, LOQ and <LOQ mean?
The certificates define LOD as limit of detection and LOQ as limit of quantitation. In plain language, LOD is the laboratory’s detection threshold and LOQ is the level at which it reports a quantitative measurement. A result shown as <LOQ is below that report’s quantitation limit; it is not a numerical concentration.
For the synthetic-tryptamine panel, the 4-AcO-DET LOQ is 0.000159928% for Strawberry Dream, 0.000147652% for Blue Raspberry, 0.000148832% for Watermelon Wonder, and 0.000148167% for Sour Tropical. The 4-AcO-DMT LOQ is 0.00016247%, 0.000149999%, 0.000151198%, and 0.000150522%, respectively. Each corresponding result is <LOQ.
Why do 4-AcO-DET and 4-AcO-DMT matter here?
On December 11, 2025, the California Department of Public Health warning said laboratory-tested TRE House Magic Mushroom gummies, chocolate bars and syrup contained illegal psychedelic compounds. CDPH said all products it tested contained 4-Acetoxy-DET (4-AcO-DET), while most also contained 4-Acetoxy-DMT (4-AcO-DMT), and its warning applied to all products regardless of lot number or package date.
CDPH named Watermelon Wonder, Sour Tropical and Strawberry Dream gummies among the products it said were laboratory tested and determined to be adulterated. That December 2025 state warning and the July 2026 certificates concern different testing events. For a bag in hand, the certificate to read is the one whose batch matches the bag; CDPH says its December 11, 2025 warning applies to the products it named regardless of lot numbers or dates on the packaging.
What can a certificate tell you—and what should you still check?
A certificate can identify the product and batch named on the report, the date, the laboratory, the analytes and contaminant panels tested, the laboratory’s reporting limits, and the result recorded for the analyzed sample. It is most useful when the flavor and batch number both match your package.
The FDA explains that it does not have the authority to approve dietary supplements for safety and effectiveness before they are sold. A certificate is a batch record to match and read; it is not FDA approval.
It cannot turn a different batch, flavor, older package or unrelated product into the tested sample. It also does not answer every ingredient question by itself. For how lab findings differ from evidence in people, see this guide to human studies, lab studies and tradition. A product described as “mushroom gummies” can refer to very different formulas; compare the package label with the matching report instead of assuming the name identifies the contents.
How do you match your bag to the report?
- Find the batch or lot marking on the bag.
- Open TRE House’s lab-report page and select the report for that flavor.
- Compare the batch character by character, including the flavor code and number.
- Confirm the product name and report completion date at the top of the certificate.
- Read the named panels and results rather than relying on a general “tested” label.
Keep your package and certificate together if you need to ask the seller about a batch. If effects or symptoms are a concern, write down the product, flavor, batch, amount and timing to bring to a clinician. A practical health record should center your symptoms and daily function; whole-person health goals can help organize that conversation.
Before you rely on a mushroom-gummy lab report
- Match the exact batch, not just the brand or flavor.
- Check the completion date and laboratory named on the certificate.
- Read what the panel tested and what <LOQ means for that report.
- Remember the December 11, 2025 CDPH warning covers the TRE House Magic Mushroom gummies, chocolate bars and syrup it named, regardless of lot number or date information on packaging.
- Ask the seller for the matching certificate if your bag has a batch that is not listed.
By the Integrative Health Evidence Guide Team