Philips recalls CombiDiagnost R90 Stitching Patient Support model 709030 due to risk of footplate falling and causing injury during use. Affected units have specific serial numbers.
The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
Philips is recalling CombiDiagnost R90 Stitching Patient Support devices because the footplate can fall or swing down, potentially injuring the operator or patient. This recall affects specific units with serial numbers SN17000130 and SN17000018.
The hook that holds the footplate in place does not secure it vertically. This means the footplate could fall or swing downward, which might injure the operator or patient during use.
Healthcare professionals using the CombiDiagnost R90 device for stitching patient support are most at risk. Patients using this device during procedures may also be affected.
Check for the CombiDiagnost R90 Stitching Patient Support model 709030 with serial numbers SN17000130 or SN17000018. This device is used in medical settings for patient stitching procedures.
Look for the serial numbers SN17000130 or SN17000018 on the device to confirm if it is affected.
The specific model is CombiDiagnost R90 Stitching Patient Support with serial numbers SN17000130 and SN17000018.
Check if your device has the serial numbers SN17000130 or SN17000018 for the CombiDiagnost R90 Stitching Patient Support model 709030.
The recall record does not specify a remedy, so contact Philips Medical Systems for guidance on next steps.
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-2847-2018 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-2847-2018 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.
