Philips recalls EasyDiagnost Eleva DRF Stitching Patient Support model 706032 due to risk of footplate falling and causing injury. Affected units have specific serial numbers listed in the recall notice.
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 EasyDiagnost Eleva DRF Stitching Patient Support model 706032 because the hook may not hold the footplate securely, causing it to fall and potentially injure the operator or patient. This is a safety hazard that requires immediate attention to prevent injury.
The hook in the device does not securely hold the footplate in the vertical position. This can cause the footplate to fall or swing downward, potentially injuring the operator or patient during medical procedures.
Healthcare professionals using the EasyDiagnost Eleva DRF Stitching Patient Support device for medical procedures are most at risk. Patients and operators could be injured if the footplate falls during use.
Check for the model number 706032 on the device. Affected units have specific serial numbers listed in the recall notice, including 470350/SN10000103 and others.
Verify if your EasyDiagnost Eleva DRF Stitching Patient Support has the model number 706032 and the listed serial numbers.
The recalled model is EasyDiagnost Eleva DRF Stitching Patient Support 706032.
Affected units include serial numbers like 470350/SN10000103, 482735/SN11000053, and others listed in the recall notice.
The recall record does not specify a remedy, so no action is required beyond checking if your device is affected.
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-2867-2018 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-2867-2018 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.
