Retatrutide testing and lab results

Every dashboard panel uses the same 18,764-entry Retatrutide aggregate, updated on 2026-10-18. Published entries have a recorded purity or amount-deviation value. Entries are stored results, not unique certificates or batches. Reviewed seller-code aliases are included. The median uses 18,740 numeric purity values, including recorded zero; it does not use entries missing purity.

The amount comparison uses 12,076 entries with a usable tested amount versus an explicit label amount. Below range is strictly less than −10%; within range includes −10% and +10%; above range is greater than +10%. Finnrick batch-claim comparisons are excluded because their reference is not consistently the vial label. A result above label is still a deviation, not a benefit.

The purity chart uses non-overlapping bins. “Below 99%” excludes the highest bin and rescales the bars against the remaining count. Recorded zero can reflect how the source stored a non-detection or zero-amount finding; read the original report before interpreting it as a conventional purity result. Findings can overlap across different tests and cannot be added together. Percentages are rounded.

Vendors with reports counts distinct stored vendor identities attached to these entries, not reviewed or verified businesses. Aliases, unresolved identities and later merges can affect this count. 444 entries have no linked vendor identity. This full-archive count is separate from the selected vendors below.

Lab names use the public lab-attribution rules. 361 entries have no attributable testing lab; these are shown separately and do not increase the 20-lab total. Finnrick's lettered labs are its anonymized partner-lab labels.

Monthly activity uses 18,704 valid test dates and 60 discovery dates where a valid test date is unavailable. 0 entries have no usable date. Months with no included entries are retained; the current month is incomplete. Activity measures the records collected, not sample quality or market-wide testing.

Endotoxin results show the verdict recorded in each source report within this same archive cohort. Recorded but unclassified results and missing data are separate; neither counts as a pass. Bare numeric readings do not imply a verdict without the applicable report specification. Endotoxin-only records without purity or amount data fall outside this archive cohort.

These are voluntary public tests of submitted samples, not a random survey of the market. Sterility and measured zero amount are separate measures not loaded here. Clinical papers in the research column are a separate evidence source and do not validate seller products.