FDA recall Z-0399-2019

Zimmer Biomet, Inc. · Class II · device

Product

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.

Reason for recall

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

Distribution

US Nationwide Distribution in the states of: AZ, FL, MI, OH, VA & WI

Key facts

Status
Terminated
Initiation date
2018-09-21
Report date
2018-11-14
Termination date
2020-04-14
Voluntary/Mandated
Voluntary: Firm initiated
Location
Warsaw, IN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0399-2019