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Zimmer, Inc. recalls Trilogy II Constrained Liner The Trilogy Longevity Constrained Liner serves as the articular surface for a femoral
Recalled November 28, 2012 · FDA recall Z-0386-2013 · Zimmer
Hazard
Trilogy Longevity Constrained Liner devices were packaged in incorrect cartons. The product is packaged in the incorrect carton. Product labels and patient labels are correct, matching the product inside the carton. · FDA Class II
Units
1
Sold at
USA (nationwide) including the states of Ohio, Carolinas and New England.
Description
Trilogy Longevity Constrained Liner devices were packaged in incorrect cartons. The product is packaged in the incorrect carton. Product labels and patient labels are correct, matching the product inside the carton.
Product
Trilogy II Constrained Liner The Trilogy Longevity Constrained Liner serves as the articular surface for a femoral head in total hip arthroplasty.
Manufacturer(s)
Zimmer, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →