Philips recalls CombiDiagnost PCF software v1.0.5 for error 80 locking geometry and incorrect thermos switch installation. Affected units may require service engineer intervention.
When using the Table Up/Down button, the system may experience Error 80, which locks the geometry in that specific state, requiring the intervention of a service Engineer. Additionally, the thermos switch, which handles power down of the unit in case of transformer overheating, was installed incorrectly at production.
Philips is recalling CombiDiagnost PCF software version 1.0.5 due to potential geometry locking during use and incorrect thermos switch installation. This could require service engineer intervention to fix.
The Table Up/Down button may cause Error 80, locking the system geometry and requiring service engineer intervention. The thermos switch, which handles power down during transformer overheating, was installed incorrectly at production.
Medical facilities using the CombiDiagnost PCF X-ray system with software version 1.0.5 are affected. Staff operating the system are most at risk during use.
Check for software version 1.0.5 on CombiDiagnost PCF X-ray systems. Product codes include SN374, SN17081704, SN17121782, SN18011800, SN18081862, SN18061846, SN18111907.
Reach out to Philips Medical Systems for service engineer assistance with the software issue or thermos switch correction.
Software version 1.0.5 of CombiDiagnost PCF.
Error 80 may lock the system geometry, and the thermos switch was installed incorrectly at production.
Check for product codes SN374, SN17081704, SN17121782, SN18011800, SN18081862, SN18061846, or SN18111907.
We’ve drafted a message you can send Philips Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-1329-2020 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-1329-2020 from Philips Medical Systems. 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.
