Philips recalls DigitalDiagnost Dual Detector (Stitching Patient Support) 712022 with serial numbers listed. The footplate may fall or swing down, risking injury to operator or patient. Stop using immediately.
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 its DigitalDiagnost Dual Detector (Stitching Patient Support) model 712022 due to a risk that the footplate could fall or swing down, potentially injuring the operator or patient. This recall affects specific units with the listed serial numbers.
The hook that holds the footplate in place does not securely fasten it vertically. This can cause the footplate to fall or swing downward, which may lead to injury for both the operator and the patient during medical procedures.
Healthcare professionals using the DigitalDiagnost Dual Detector for medical procedures and patients receiving treatment with this device are at risk. Operators and patients could be injured if the footplate falls or swings down.
This recall applies to DigitalDiagnost Dual Detector (Stitching Patient Support) 712022 with specific serial numbers listed in the record. Check the serial number on the device to see if it matches the numbers provided.
Discontinue use of the DigitalDiagnost Dual Detector (Stitching Patient Support) 712022 if it has the listed serial numbers.
The recalled model is DigitalDiagnost Dual Detector (Stitching Patient Support) 712022.
Check the serial number on your device against the list of affected serial numbers provided in the recall notice.
The recall record does not mention any remedy or replacement options.
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-2859-2018 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-2859-2018 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.
