Philips recalls DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081 due to footplate safety risk. Affected units may cause injury if footplate falls or swings down during use.
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 DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081 because the footplate can fall or swing down, potentially injuring the operator or patient. This is a safety issue that requires immediate attention to prevent harm.
The hook that holds the footplate in place does not secure it vertically. This means the footplate can fall or swing downward, which could cause injury to the operator or patient during use.
Healthcare professionals using the DigitalDiagnost 2.x Upgrades for stitching patient support are most at risk. Patients and operators using the affected units could be injured if the footplate falls or swings.
Check for the DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081 with serial numbers 428633/SN09000234, 430908/SN09000165, or 487800/SN11000531. These units were sold with the specific model and serial numbers listed.
Immediately stop using the affected DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081 units as they pose a risk of injury.
The recalled product is Philips DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081.
The affected units have serial numbers 428633/SN09000234, 430908/SN09000165, and 487800/SN11000531.
Check if your unit has the specific serial numbers listed: 428633/SN09000234, 430908/SN09000165, or 487800/SN11000531.
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-2848-2018 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-2848-2018 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.
