FDA Medical Device Recall Enforcement Quarterly Archive is a versioned Zentra Foundry digital download. Delivery is an immediate Gumroad download after a successful one-time purchase. No Zentra subscription or customer API account is required. What it is Immutable normalized edition of current-quarter FDA medical-device recall enforcement reports with classification, firm, product, reason, distribution, and first-party evidence fields. This is a reference archive, not an alerting service. Who it is for Teams that need repeatable public-data monitoring without manual copy-paste workflows. Builders packaging public signals into datasets, APIs, automation, or agent tools. Operators who need a reliable way to inspect, compare, and use public-data products. Device quality and post-market teams who need a frozen quarterly FDA medical-device recall enforcement edition they can checksum and cite. What you get One immutable ZIP for this edition, including: README.md — buyer-readable setup and file map Sample records for format review JSON Schema and Product Output Contract Source / provenance notes Quality, health, and smoke evidence LICENSE.md CHANGELOG.md SHA-256 checksums.json Update cadence: Snapshot-driven. A labelled sample and schema preview are available on the Foundry product page before purchase. Schema fields recall_number — Recall number. report_date — Report date. recall_initiation_date — Recall initiation date. classification — Classification. status — Status. recalling_firm — Recalling firm. product_description — Product description. reason_for_recall — Reason for recall. product_quantity — Product quantity. distribution_pattern — Distribution pattern. voluntary_mandated — Voluntary or mandated. country — Country. state — State. source_url — Source URL. Source and provenance Public source URL shown in the sample: https://api.fda.gov/device/enforcement.json. Provenance: Foundry product package / ProductStudio public-safe metadata. Current Gumroad edition label: 2026-Q3.f90d4585599f. Limitations This is a packaged public-data snapshot, not legal, medical, safety, or regulatory advice. Samples and schemas document the delivered format. Source-backed editions are bounded by their recorded capture and source terms. Synthetic or fixture rows are labelled when present. The product does not guarantee business, legal, compliance, security, procurement, or model outcomes. Buyers remain responsible for checking current source terms and using the data in line with those terms. Foundry page, support, refunds Foundry product page: https://zentrafoundry.com/datasets/fda-medical-device-recall-enforcement-quarterly-archive Support: ops@nimblique.studio Refunds: Gumroad 14-day policy at checkout. Statutory rights remain unaffected.