FDA Enforcement Class II Terminated

Product 33 consists of all product under product code: JDI and same usage: Item no: 662406515 HGP II ACETABULAR CUP BON 662406520 HGP II ACETABULAR CUP BON 662406525 HGP II ACETABULAR CUP BON 662406530 HGP II ACETABULAR CUP BON 662406535 HGP II ACETABULAR CUP BON 662406540 HGP II ACETABULAR CUP BON 662406550 HGP II ACETABULAR CUP BON 662406560 HGP II ACETABULAR CUP BON For use in total hip arthroplasty

Recall: Z-1131-2016 · Reported March 23, 2016

Enforcement

Recall Number
Z-1131-2016
Event ID
72900
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Zimmer Manufacturing B.V.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
March 23, 2016
Initiation Date
January 11, 2016
Classification Date
March 12, 2016
Termination Date
April 13, 2017
Address
Turpeaux Industrial Park Rd 1 km 123.4, Mercedita, PR, 00715, United States

Description

Product 33 consists of all product under product code: JDI and same usage: Item no: 662406515 HGP II ACETABULAR CUP BON 662406520 HGP II ACETABULAR CUP BON 662406525 HGP II ACETABULAR CUP BON 662406530 HGP II ACETABULAR CUP BON 662406535 HGP II ACETABULAR CUP BON 662406540 HGP II ACETABULAR CUP BON 662406550 HGP II ACETABULAR CUP BON 662406560 HGP II ACETABULAR CUP BON For use in total hip arthroplasty

Reason

As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.

Code Info

lot no.: 61674472 61906696 62016799 62332483 61674473 61902194 61906697 62326386 61674476 61953546 62161131 62172656 62326385 61953547 62011539 62017894 62130757 61886072 61953548 62017895 62172659 61886073 61948763 61953551 62172661 61874793 61948764 61996232 62017897 62172663 61874794 61953554 62286122

Distribution

US Nationwide Distribution

Quantity

2236