{ "dataType": "CVE_RECORD", "dataVersion": "5.1", "cveMetadata": { "cveId": "CVE-2024-12248", "assignerOrgId": "7d14cffa-0d7d-4270-9dc0-52cabd5a23a6", "state": "PUBLISHED", "assignerShortName": "icscert", "dateReserved": "2024-12-05T15:20:44.585Z", "datePublished": "2025-01-30T18:17:22.814Z", "dateUpdated": "2025-02-12T16:53:16.892Z" }, "containers": { "cna": { "affected": [ { "defaultStatus": "unaffected", "product": "CMS8000 Patient Monitor", "vendor": "Contec Health", "versions": [ { "status": "affected", "version": "Firmware version smart3250-2.6.27-wlan2.1.7.cramfs" }, { "status": "affected", "version": "Firmware version CMS7.820.075.08/0.74(0.75)" }, { "status": "affected", "version": "Firmware version CMS7.820.120.01/0.93(0.95)" } ] } ], "credits": [ { "lang": "en", "type": "finder", "value": "An anonymous researcher reported these vulnerabilities to CISA." } ], "descriptions": [ { "lang": "en", "supportingMedia": [ { "base64": false, "type": "text/html", "value": "
Contec Health CMS8000 Patient Monitor is vulnerable to an out-of-bounds write, which could allow an attacker to send specially formatted UDP requests in order to write arbitrary data. This could result in remote code execution.
Per FDA recommendation, CISA recommends users remove any Contec CMS8000 devices from their networks.
Please note that this device may be re-labeled and sold by resellers. For a list of known re-labeled devices, please refer to FDA's safety communication.
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