Philips recalls DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031 with serial numbers SN15000196, SN15000180, SN15000282, SN15000281, SN15000192, and SN15000189 due to risk of footplate falling and causing injury to operator or patient.
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 recalls specific models of DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031 because the footplate can fall or swing down, potentially injuring the operator or patient. This recall affects only the listed serial numbers and requires immediate attention to prevent injury.
The hook that holds the footplate in place does not secure it vertically. This can cause the footplate to fall or swing downward, potentially injuring the operator or patient during use.
Healthcare professionals using the DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031 device are most at risk. Patients using the device may also be affected if the footplate falls.
Check if your device has the serial numbers SN15000196, SN15000180, SN15000282, SN15000281, SN15000192, or SN15000189. The product is a DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031.
Look for the serial numbers SN15000196, SN15000180, SN15000282, SN15000281, SN15000192, or SN15000189 on your DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031 device.
Check if your device has the serial numbers SN15000196, SN15000180, SN15000282, SN15000281, SN15000192, or SN15000189. If so, it is affected.
The recall record does not specify a remedy, so contact Philips Medical Systems for further instructions.
The recall record does not provide a remedy, so it is not safe to continue using the device without checking with Philips Medical Systems.
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-2843-2018 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-2843-2018 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.
