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FDAFDA · Food and drugs·Recall number Z-0399-2019

StageOne Hip, Models 431207 & 431209Usage: Product Usage: The single-use cement spacer molds are sterile disposables made of medical grade silicone with a 316L stainless steel reinforcement stem. They are designed to be filled with polymethylmethacrylate/gentamicin bone cement, or equivalent, by injecting with a dispenser/gun into the mold. After the cement cures, the temporary spacers are to be removed from the molds with the reinforcement remaining as the core of the spacer, and placed into the joint space. The spacers remain in place (180 days or less) until the second stage of the two-stage procedure is performed to implant a conventional hip joint prosthesis.

Published November 14, 2018 · Recall initiated: September 21, 2018

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

There is a potential for comingling of the 43MM and 51 MM molds

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Zimmer Biomet, Inc.
Distributor
US Nationwide Distribution in the states of: AZ, FL, MI, OH, VA & WI
Lot
Item Number 431207 Lot # 705550, UDI - (01)00880304447165(17)270927(10)705550 Item Number 431209 Lot # 705570, UDI - (01)00880304447141(17)270916(10)705570 Lot # 705580, UDI - (01)00880304447141(17)270916(10)705580
Risk classification
Class II
Area (FDA)
device
Country
United States

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