Philips recalls DigitalDiagnost Release 3 Stitching Patient Support models with serial numbers 510694/SN12000240 to 511346/SN13000008. The footplate may fall or swing, risking 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 its DigitalDiagnost Stitching Patient Support devices because the footplate can fall or swing, potentially injuring the operator or patient. This recall affects medical devices used in clinical settings where precise patient positioning is critical.
The footplate is not securely held in the vertical position, so it can fall or swing downward. This movement could injure the operator or patient during medical procedures requiring precise patient positioning.
Healthcare professionals using Philips DigitalDiagnost Release 3 Stitching Patient Support devices for medical procedures are most at risk. Patients and operators during procedures could be injured if the footplate falls or swings.
Check for the model name 'DigitalDiagnost Release 3 (Stitching Patient Support)' with serial numbers listed in the recall notice. The affected units have specific serial numbers starting with 510089 to 511346.
Look for the serial number on the device label to confirm if it matches the recalled numbers listed in the notice.
Reach out to Philips Medical Systems for guidance on next steps if your device is affected.
The footplate does not securely hold the device in the vertical position, which can cause it to fall or swing, potentially injuring the operator or patient.
The affected models have serial numbers starting with 510089/SN12000293 to 511346/SN13000008 as listed in the recall notice.
The recall does not require immediate stop use; however, healthcare professionals should check if their device is affected and contact Philips for guidance.
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-2844-2018 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-2844-2018 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.
