Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0936-2014 — The Symbionic Leg is an integrated prosthetic leg for transfemoral and knee disarticulation amputees. The prosthesis is composed of the RHEO KNEE and the PROPRIO FOOT, both already existing products from ¿ssur. Both are a battery powered micro-processor controlled prosthetic device and are conne

U.S. FDA — Device Enforcement · United States · 2012-02-12 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0936-2014
Date of alert: 2012-02-12
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Ossur Americas, Inc.
Product category: device
Product type: Devices

Reported risk: OSSUR initiated this recall of the Symbionic Leg because it may have a possible defect in a small batch of electronics.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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