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Terminated

The Rheo Knee bionic prosthetic is to be used exclusively for fittings of lower extremity amputations. RHEO KNEE uses Artificial Intelligence to continuously adapt to the users walking style and environment. The RHEO KNEE recognizes and responds immediately to changes in speed, load and terrain, restoring the users ability to walk naturally, comfortably and confidently at any speed.

FDA Recall Z-1322-2015 · Posted 2015-03-25

Recalling FirmOssur H / F
Recall StatusTerminated
Product CodeISW
Date Initiated2015-02-26
Date Terminated2015-11-20
Product Quantity4715 units (2 units affected)

Reason for Recall

The firm is recalling Rheo Knee bionic prosthetic due to it being discovered during an internal audit of the service line that devices were released for distribution without fully going through the assembly process.

Firm Action

The firm, Ossur, notified their customers of the Recall Notice via phone on February 26, 2015. The firm informed the customers about the recalled product, the problem and actions to be taken. The customers were instructed to send the unit in for service so the Acceptance testing can be performed for the unit in accordance to their process. If you have any questions, please contact Regulatory Affairs & Quality Assurance specialist at 949-382-3741 or email: [email protected].

Root Cause

Employee error

Distribution Pattern

Worldwide distribution: US distribution in TN and country of: Austria.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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