CISA ADP Vulnrichment

Answer in brief

CVE-2026-88624 records a Critical severity (CVSS 9.1) vulnerability in CISA ADP Vulnrichment. The current sources do not mark it as known exploited. The current feed maps n/a/n/a (generic). Check affected ranges and fixed versions before updating.

Analysis pending evidence review

HOL Guard separates source facts from reviewed analysis. See the methodology.

Published Sep 22, 2026Updated Sep 23, 2026Source checked Sep 23, 2026First seen by HOL Sep 22, 2026Material review Sep 23, 2026

Upstream Advisory

Key facts

Risk: Critical · CVSS 9.1
Exploitation: Not marked as known exploited
Affected software: 1 mapped package or product
Fix availability: Not reported

Why this deserves its current priority

CVSS is 9.1. The current sources do not mark it as known exploited. Treat this as a source-backed prioritization signal, not a statement about your environment.

Analysis status

Analysis pending evidence review

Factual feed record only; HOL analysis is not approved for indexing. Read the methodology.

Affected scope and exposure questions

The current feed maps n/a/n/a (generic). Check affected ranges and fixed versions before updating.

Mapped affected packages and fixed versions
Package	Affected range	Fixed version
n/a/n/ageneric	n/a	Not reported

Recommended response

Check inventory. Check lockfiles and deployed manifests for n/a/n/a.
Review the reported fix. Monitor this advisory for an available fix and review any installs of the affected package.

Evidence timeline and material changes

Published upstream
Sep 22, 2026
Evidence: source:cvelist:source_dates:source-dates:record
Source modified
Sep 23, 2026
Evidence: source:cvelist:source_dates:source-dates:record
First seen by HOL
Sep 22, 2026

Sources and claim methodology

GitHub security advisorygithub.com

Upstream source description

Missing path validation in the Worktree.remove component of openCode v1.18.26 allows attackers to execute arbitrary recursive directory deletion via a crafted payload.

Quoted source text, attributed separately from HOL analysis.