ProductGuru Recalls

Official recall record

Power Knee, REF: PKA10001, and PKA10003; with Power Knee Battery, REF: PKA10002

US FDA — Medical Devices · 2023-12-26 · IcelandClass II
Issuing authority
US FDA — Medical Devices
Recall initiated by firm
2023-12-26
Country of alert
Iceland
Alert level
Class II
Alert type
recall
Barcode (EAN/GTIN)
05690967648381
Brand on record
Ossur H / F

What the authority reported

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.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.