Ossur H/F recalls Power Knee devices (PKA10001, PKA10003) with Power Knee Battery (PKA10002) due to risk of unexpected shutdown causing loss of support and potential fall. Check serial numbers for affected units.
Knee batteries may need replacement with conforming batteries to ensure there isn't a failure to turn on the device, or an unexpected shutdown, which is a momentary loss of power to the knee where the user may experience loss of support that can lead to a fall and potential injury.
Ossur is recalling Power Knee devices with specific battery models because the batteries may fail to turn on properly or shut down unexpectedly. This could cause a loss of support and lead to a fall if the user is not properly supported.
The batteries may fail to turn on or shut down unexpectedly, causing a temporary loss of power to the knee device. This loss of support could result in the user falling if they are not properly stabilized.
Users of Ossur Power Knee devices with the specific battery models (PKA10002) and the listed serial numbers are affected. Individuals who rely on these devices for mobility support are most at risk.
Check for the Power Knee device model numbers PKA10001 or PKA10003 with the Power Knee Battery model PKA10002. Affected units have specific serial numbers listed in the recall notice.
Look for the device and battery serial numbers listed in the recall notice to confirm if your unit is affected.
No, the recall does not require immediate stop use. However, you should check if your device is affected and follow the action steps.
The recall does not specify a remedy, so you should contact Ossur H/F directly for guidance on next steps.
Check the device and battery serial numbers against the list provided in the recall notice.
We’ve drafted a message you can send Ossur H / F to request your refund or repair — edit it as you like.
Subject: Recall Z-0788-2024 — Ossur H / F Ossur H / F Hello, I own a Ossur H / F that is covered by recall Z-0788-2024 from Ossur H / F. 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.
