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The business of physical AI.

Corrections

DEPLOY operates corrections as standard editorial practice, not exception. When primary-source verification surfaces a correction to previously-shipped framings, the correction surfaces transparently with the verification evidence cited at primary-source verification depth.

The canonical corrections journal lives on the registry property at registry.deploy.report/corrections. The corrections journal operates as the structural corrections-data surface with IncidentStatusEvent + RegulationStatusEvent journaling. This page references the news-pub-lane framework-in-action correction-as-worked-example narratives that compound the structural corrections data with narrative depth.

Data-quality corrections

Specific registry records corrected to primary-source-anchored evidence. Each entry names the prior assertion, the corrected fact, the primary source, and the corrected registry records.

  • Corrected 2026-06-05

    da Vinci instrument arm diagnostic recall is a 2026 event, not 2025

    Prior: The da Vinci instrument arm diagnostic recall was indexed under a 2025 slug on both the regulatory filing and the incident record. The event was treated as a 2025 incident across registry cross-links.

    Correction: The recall is a 2026 event. FDA assigned recall Z-1232-2026 to the diagnostic-error correction and posted the record on 2026-02-02. Registry slugs re-anchored: the regulatory filing moved from fda-recall-davinci-instrument-arm-diagnostic-2025 to fda-recall-davinci-instrument-arm-diagnostic-2026; the incident moved from davinci-instrument-arm-diagnostic-recall-2025 to davinci-instrument-arm-diagnostic-recall-2026.

    Primary source: FDA recall Z-1232-2026

    Records: Registry incident record; Registry regulatory filing record; Phase 3 Dim 3 supply-chain component failure mode framework-in-action

  • Corrected 2026-06-05

    Intuitive Ion recall landscape: 4 verified FDA records, no 2025 entry

    Prior: The Intuitive Ion robotic bronchoscopy platform carried a 2025 recall reference in the registry under the slug fda-recall-intuitive-ion-2025, and the companion incident was indexed as intuitive-ion-recall-2025. The 2025 anchoring did not resolve against any FDA recall record.

    Correction: No 2025 Ion recall exists. The fda-recall-intuitive-ion-2025 slug is deprecated and the incident slug re-anchored from intuitive-ion-recall-2025 to intuitive-ion-recall-2020. Agent A verified four Ion-related FDA records via openFDA: Z-0489-2021 (catheter, FDA posted 2020-12-02), Z-0106-2022 (Flexision biopsy needle, FDA posted 2021-10-20), Z-2720-2024 (filed 2024-08-23), and Z-1134-2026 (filed 2026-01-21). The earlier res.cfm pointer URLs (209213 and 188906) are retired or 404 and stay at honest-absence; the openFDA records are the verification anchor.

    Primary source: openFDA recall database

    Records: Registry incident Z-0489-2021 (catheter); Registry incident Z-0106-2022 (Flexision biopsy needle); Registry incident Z-2720-2024; Registry incident Z-1134-2026

  • Corrected 2026-06-05

    Wing Part 135 certification is 2019, not 2022; Matternet Part 135 record deprecated

    Prior: Wing's Part 135 air carrier certification was anchored to 2022 in the registry under the slug faa-part135-wing-2022. Matternet was anchored to a 2022 Part 135 record under the slug faa-part135-matternet-2022.

    Correction: Wing received Part 135 certification in October 2019 per the FAA. The Wing record re-anchored to faa-part135-wing-2019. Matternet has no Part 135 certification; faa-part135-matternet-2022 is deprecated. The real Matternet FAA record is a Type Certificate (faa-type-cert-matternet-m2-2022; Type Cert September 2022, Production Cert 2022-11-30). Matternet's operational exemption (Section 44807) stays at honest-absence: no corroborable standalone exemption number; we do not assert one.

    Primary source: FAA Part 135 certification record

    Records: Registry Wing Part 135 record (2019); Registry Matternet M2 Type Certificate (2022); Matternet registry record

Framework-in-action correction narratives

Each correction-narrative documents a specific catch at narrative-canonical depth: how the catch happened + what discipline surfaced it + what editorial outcome resulted + what broader pattern emerges. The narratives operate as canonical worked examples of the framework discipline at editorial-anchor depth.

  • Entity-type discipline

    1X Redwood is a captive brain, not humanoid hardware

    Dispatch framed Redwood as humanoid hardware sibling to NEO; registry verification confirmed brain entity at /brains/1x-redwood. Editorial scope corrected at brain-providers cluster as captive-brain archetype canonical worked example.

  • Entity-distinction discipline

    Physical Intelligence at $5.6B, not $11B

    Aggregator coverage cites PI valuation at $11B; per Agent A primary-source verification PI is at $5.6B confirmed. $10B and $38B figures belong to Project Prometheus separate Bezos lab. Adjacent positioning produces conflation pressure.

  • Corporate-state precision

    Covariant continuing-but-diminished, not acquired by Intrinsic or defunct

    Two opposing aggregator framings both wrong. Verified state: corporate entity continues; Ted Stinson CEO; legacy Brain via KNAPP verified commercial; non-exclusive license/IP retained. Founders + ~25% staff to Amazon AGI Aug 2024. Continuing-and-diminished simultaneously.

  • Three-layer aggregator-drift rejection

    Figure 03 at Catalyst Brands Reno, not BMW Spartanburg + Leipzig

    Spartanburg was Figure 02 (30,000 BMW X3 vehicles + 1,250 hours runtime). Leipzig went to Hexagon AEON. Figure 03 = Catalyst Brands Reno per May 2026 partnership. Three distinct deployments + three layer-conflations rejected.

  • Source-quality per-claim discipline

    Red Cat Black Widow SRR LRIP $12.9M, not $55M

    Army FOIA primary-source verification: $12.9M LRIP obligated (NOT $55M); 5,880 systems = Army OBJECTIVE (NOT OBLIGATED); Black Widow replaced Skydio (NOT Black Hornet). Short-seller report carries FOIA figures + allegation framings simultaneously; per-claim verification reads each at its source-quality depth.

  • Small-fact role identification

    Monogram's Doug Unis is CMO/founder, not CEO

    Pre-acquisition CEO Benjamin Sexson; Unis is CMO + founder. ZB acquired Monogram closed October 7, 2025 (~$168M EV + CVR). Two parallel cap-flags at Monogram entity scope: leadership identification + autonomy-classification descriptor ('semi-autonomous' ZB/trade-sourced NOT FDA-letter-verbatim).

  • Smallest-granularity small-fact discipline

    Stryker headquartered in Portage, MI, not Kalamazoo

    SEC 10-K verifies Portage. Aggregator coverage frequently defaults to Kalamazoo as regional shorthand. Small-fact discipline cuts uniformly: framework reads single-city location identification at the same primary-source verification depth as valuation corrections + role identifications.

Cross-property references

For the structural corrections journal with full incident + regulation status events, see registry.deploy.report/corrections. For the methodology canonical reference, see how DEPLOY verifies. For the editorial process documentation, see /editorial-process. For DEPLOY's funding posture, see /funding. For DEPLOY's conflicts of interest disclosure, see /conflicts.