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Health product recall

Trident Acetabular System Hemispherical Surgical Protocol and Trident Product Reference Guide (2014-09-22)

Starting date:
September 22, 2014
Posting date:
October 9, 2014
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-41695

Recalled Products   

Trident Acetabular System Hemispherical Surgical Protocol and Trident Product Reference Guide 

Reason

Stryker has received a report from the field of incorrect product information identified in Trident Surgical Protocol, LSP69 ("LSP69") and Trident Product Reference Guide, LX3PRG ("LX3PRG"). LSP69 and LX3PRG each contain the table, which references an incorrect number of screw holes for trident hemispherical ha cluster shell sizes 44mm - 50mm.

Affected products

Trident Acetabular System Hemispherical Surgical Protocol and Trident Product Reference Guide 

Lot or serial number

All lots.    

Model or catalog number

More than 10 numbers, contact manufacturer.   

Companies
Manufacturer
Howmedica Osteonics Corporation
325 Corporate Drive
Mahwah
07430
New Jersey
UNITED STATES