AMO recalls Catalys Precision Laser Systems with Windows 7 due to a remote code execution vulnerability that could allow unauthorized system access and data compromise.
Aberrometer and precision laser systems are affected by a remote code execution vulnerability existing when the Microsoft Windows Print Spooler service is enabled, and improperly performs privileged file operations. This could be exploited to run arbitrary code with SYSTEM privileges, allowing for program installation; view/change/deleting data; or creation of new accounts with full user rights.
AMO is recalling Catalys Precision Laser Systems (models Catalys-U, Catalys-I, Catalys-C) that run Windows 7. The systems have a security vulnerability that could let attackers gain full control over the device, including installing programs and accessing sensitive data.
The vulnerability exists when the Microsoft Windows Print Spooler service is enabled. Attackers could exploit this to run arbitrary code with full system privileges, allowing them to install programs, view or change data, and create new user accounts with full access.
Users of Catalys Precision Laser Systems with Windows 7 operating systems are affected. Those with the specific models listed in the recall are most at risk.
Check if your Catalys Precision Laser System has Windows 7 installed. Affected models include Catalys-U (US), Catalys-I (International), Catalys-C (China), and specific model numbers with Windows 7 Professional or Embedded Standard.
Verify your Catalys system uses Windows 7 with the specific model numbers listed in the recall.
No, only specific Catalys Precision Laser System models with Windows 7 Professional or Embedded Standard.
The recall does not specify a remedy, so no action is required at this time.
The recall states the vulnerability could allow unauthorized access to the system, but does not specify actual harm to users.
We’ve drafted a message you can send AMO to request your refund or repair — edit it as you like.
Subject: Recall Z-0444-2022 — AMO AMO Hello, I own a AMO that is covered by recall Z-0444-2022 from AMO. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
