CVE-2026-75029: ISC BIND 9 · Asymmetric Resource Consumption
Affects ISC BIND 9Source CVE Database V5
Not known to be exploited · CVSS 5.3 Medium.
Data as of 31 Oct 2026, 20:20 UTC
- EPSS
- 0.4% chance of exploitation in 30 days – higher than 41% of CVEsExploit Prediction Scoring System: the likelihood attackers will use this flaw soon.
CVSS:3.1/AV:N/AC:L/PR:N/UI:N/S:U/C:N/I:N/A:LExploitation evidence
Disclosed: evidence found.
CVE published 16 Sep 2026
Detectable: no evidence on record.
No public nuclei template indexed
Weaponized: no evidence on record.
No public exploit code indexed in Metasploit or Exploit-DB
Exploited in the wildExploited: no evidence on record.
Not in CISA KEV and no source reports exploitation
Observed by OffSeq MirageSeen by Mirage: no evidence on record.
No attack traffic recorded by OffSeq Mirage sensors
A missing step is not evidence of safety. Sources: cve.org (opens in a new tab), the Metasploit, Exploit-DB and nuclei-templates index as of 31 Oct 2026.
What to do
Affected software
| Product | Affected | Fixed in |
|---|---|---|
| ISCBIND 9 | Affected
| Fixed in– |
GitHubisc/bind9pkg:github/isc/bind9Other threats | Affected
| Fixed in– |
Check your own hosts for these packages with threat-finder (opens in a new tab), our free open-source scanner.
AI-suggested
Until an official fix is available, consider monitoring memory usage patterns for unusual spikes related to DNS query responses. No vendor advisory or patch links are provided in the current data.
Description
CVE-2026-75029 is a medium severity vulnerability in ISC BIND 9 that allows an attacker to cause asymmetric resource consumption via amplification. By sending multiple copies of a record that should only exist once in a query response, such as an SOA record with identical RDATA, the BIND server appends these to the in-memory RDATA set. This behavior increases memory usage of the negative cache and may lead to other memory-related attack vectors. The vulnerability affects multiple BIND 9 versions from 9.11.0 through 9.21.25 and their respective S1 variants.