Philips Medical recalls DigitalDiagnost Release 3 Stitching Patient Support models with serial numbers starting 492928-519609. The footplate may fall, causing 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 Medical is recalling DigitalDiagnost Release 3 Stitching Patient Support devices with specific serial numbers. The hook does not securely hold the footplate, which can fall or swing down and injure the operator or patient.
The hook in the device does not hold the footplate securely in the vertical position. This can cause the footplate to fall or swing downward, potentially injuring the operator or patient.
Users of the DigitalDiagnost Release 3 Stitching Patient Support with the listed serial numbers are affected. Medical professionals and patients using this device are at risk of injury if the footplate falls.
Check the serial number on the device. Affected models have serial numbers listed in the recall notice, such as 492928, 519609, and others.
The recalled devices have a hook that does not securely hold the footplate, so stop using the device right away to prevent injury.
The affected models are DigitalDiagnost Release 3 Stitching Patient Support with specific serial numbers listed in the recall notice, such as 492928, 519609, and others.
Check the serial number on your device. Affected models have serial numbers starting with 492928-519609 as listed in the recall notice.
Stop using the device immediately. The hook does not securely hold the footplate, which can fall or swing down and cause injury.
We’ve drafted a message you can send Philips Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2861-2018 — Philips Medical Philips Medical Hello, I own a Philips Medical that is covered by recall Z-2861-2018 from Philips Medical. 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.
