Trilogy II Constrained Liner The Trilogy Longevity Constrained Liner serves as the articular surface for a femoral head in total hip arthroplasty.
Reported: November 28, 2012 Initiated: August 27, 2012 #Z-0386-2013
Product Description
Trilogy II Constrained Liner The Trilogy Longevity Constrained Liner serves as the articular surface for a femoral head in total hip arthroplasty.
Reason for Recall
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.
Details
- Recalling Firm
- Zimmer, Inc.
- Units Affected
- 1
- Distribution
- USA (nationwide) including the states of Ohio, Carolinas and New England.
- Location
- Warsaw, IN
Frequently Asked Questions
What product was recalled? ▼
Trilogy II Constrained Liner The Trilogy Longevity Constrained Liner serves as the articular surface for a femoral head in total hip arthroplasty.. Recalled by Zimmer, Inc.. Units affected: 1.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 28, 2012. Severity: Moderate. Recall number: Z-0386-2013.
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