DOS Contract 19AQMM18R0131: Insurers Blindsided, Litigation Looms

HARTFORD, Conn. - EntSun -- INSURERS:YOU DIDN'T KNOW—AND A JURY WON'T CARE!

Insurers accepted ANAB‑issued certificates at face value, relying on the global mandate "certified once, accepted everywhere." But when ANSI‑ANAB secretly took on the role of underwriter in 2018 — a role forbidden under ISO/IEC 17011  Conformity assessment — Requirements for accreditation bodies (Example: ANSI-ANAB )accrediting conformity assessment bodies (Registrars) . The standard actively eliminates any ambiguity regarding an AB taking on commercial liability or underwriting risks through these exact sections: — every downstream policy written on those certificates became legally compromised.

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Section 4.3 — Impartiality Requirements

The Conflict: Actively underwriting or assuming financial liability for systemic or product failures means the AB inherits a direct commercial stake in the audited entity's financial survival. This structural overlap completely destroys the neutral, third-party objectivity required by this clause.

Section 5.1 — Legal and Financial Obligations

The Boundary: The standard limits liability solely to the AB's (Accreditation Body)  evaluation actions. It does not permit the AB to absorb downstream product liability or guarantee commercial outcomes, drawing a clear line that separates an evaluator from a commercial risk-bearing insurer or underwriter.

Carriers were never told.

Reinsurers were never told.

Adjusters were never told.

Legal teams were never told.

From 2018 to present, insurers unknowingly underwrote commercial liability across aerospace, medical, automotive, logistics, and manufacturing WORLDWIDE on certifications that were never valid. Now plaintiffs are arguing systemic negligence, concealment, and reliance on fraudulent accreditation — and judges are sending these cases to juries.

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Punitive damages in these cases routinely exceed compensatory damages by 5 to 50 times, turning every affected policy into a potential nuclear verdict.

Conclusion

If you received any implant manufactured after September 4, 2018, the truth is not complicated:

You cannot verify what was put inside your body.

A fraudulent accreditation environment destroys the chain of custody, the material identity, the manufacturing controls, and the legal validity of every certificate tied to your device. When the certification collapses, the implant collapses with it — legally, medically, and commercially.

From 2018 forward, every device placed into a human body was built on paperwork that was never valid.

Every carrier that insured it was exposed.

Every reinsurer that backed it was exposed.

Every hospital that implanted it was exposed.

Every surgeon who relied on those certificates was exposed.

This is not a recall.

This is not a defect notice.

This is a systemic failure of custody and verification that reaches directly into the human body and stays there.

Notification delivered.
Liability triggered.
Silence no longer an option.