Philips Medical recalls BrightView X model 882478 handcontrollers that may move unexpectedly after button release. Affected units have specific serial numbers. Stop using immediately to prevent unintended motion.
An issue with the handcontroller may result in either spontaneous uncommanded motions or continued motion after the buttons were released.
Philips Medical is recalling BrightView X handcontrollers with model number 882478 that may move unexpectedly after button release. This could cause unintended movements during medical procedures, potentially leading to injury if not addressed.
The handcontroller may move spontaneously or continue moving after buttons are released. This could cause unintended movements during medical procedures, potentially leading to injury if the device is used without proper control.
Medical professionals using the BrightView X handcontroller for surgical procedures are most at risk. Owners of the recalled model with specific serial numbers should check if their device is affected.
Check for the model number 882478 on the device. Affected units have specific serial numbers listed in the recall notice, including many starting with '110000' or '113400'.
The recalled handcontrollers may move unexpectedly after button release, so stop using them to prevent unintended motion during medical procedures.
The model number is 882478.
Check for the model number 882478 and look for specific serial numbers listed in the recall notice, including many starting with '110000' or '113400'.
The recall record does not specify a return process, so contact Philips Medical directly for instructions.
We’ve drafted a message you can send Philips Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2010-2019 — Philips Medical Philips Medical Hello, I own a Philips Medical that is covered by recall Z-2010-2019 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.
