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

Recall Z-1206-2014 — REF 623411 R S-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented (with Pin), Right, Small, Sterile R Qty 1 The S-ROM Hinged knee femoral component is used in revision surgeries when there is significant bone loss or ligament instability and additional support is needed. S-Rom femorals

U.S. FDA — Device Enforcement · United States · 2014-02-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1206-2014
Date of alert
2014-02-24
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
DePuy Orthopaedics, Inc.
Product category
device
Product type
Devices
Reported risk: DePuy Orthopaedics has identified the potential for holes to develop in the inner and outer flexible pouches that form the sterile barrier for S-ROM Noiles Rotating Hinge Femur with Pin devices. The outer carton and shrink wrap are intact. A package redesign is underway to resolve this issue. S-ROM Noiles Rotating Hinge Femur with Pin devices will remain in US Distributors inventory during the pa
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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