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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