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Class 2 Device Recall Exactech Vantage |
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Date Initiated by Firm |
November 21, 2023 |
Date Posted |
January 18, 2024 |
Recall Status1 |
Open3, Classified |
Recall Number |
Z-0588-2024 |
Recall Event ID |
93507 |
Product Classification |
Prosthesis, ankle, uncemented, non-constrained - Product Code NTG
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Product |
Exactech Vantage Mobile Bearing Tibial Inserts, Catalog Numbers: a) 350-41-23, b) 350-42-03 |
Code Information |
a) 350-41-23, GTIN none, Serial Numbers: A658148;
b) 350-42-03, GTIN none, Serial Numbers: A688867, A688880, A688864, A688868, A688870, A688872, A688873, A688876, A688879, A688881, A688882 |
Recalling Firm/ Manufacturer |
Exactech, Inc. 2320 Nw 66th Ct Gainesville FL 32653-1630
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For Additional Information Contact |
352-377-1140
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Manufacturer Reason for Recall |
Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.
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FDA Determined Cause 2 |
Packaging change control |
Action |
Exactech issued an URGENT MEDICAL DEVICE RECALL notice to its direct consignees on 11/21/2023 via email. The notice explained the issue, clinical impact, and requested the removal and return of all affected products. 11/22/2023, the firm initiated the recall OUS also by email. |
Distribution |
US NY, TX, IN, IL, MN, KY, VA, MD, TN, GA, NH, ME, SC, NV, FL, AR and Australia, Brazil, Chile, France, Germany, Guatemala, Italy, Japan, Korea, Slovenia, Spain, UK
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Total Product Life Cycle |
TPLC Device Report
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
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