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FDAFDA · Food and drugs·Recall number Z-2810-2015

Trident 10 degrees X3 Insert 36 mm ID Catalog #623-10-36I Hip implant component

Published September 30, 2015 · Recall initiated: June 25, 2015

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

it was discovered that item 623-10-36I Lot 3Y0KHP, although meeting all device specifications, was determined to be unacceptable due to a documentation issue. However the parts were inadvertently shipped to the field.

What to do

Voluntary: Firm initiated · E-Mail

Recall details

Manufacturer
Stryker Howmedica Osteonics Corp.
Distributor
Distributed in WI.
Lot
Lot Code 3Y0KHP
Risk classification
Class II
Area (FDA)
device
Country
United States

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