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U.S. Department of Health and Human Services

Class 2 Device Recall Exactech AcuMatch

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 Class 2 Device Recall Exactech AcuMatchsee related information
Date Initiated by FirmNovember 21, 2023
Date PostedJanuary 18, 2024
Recall Status1 Open3, Classified
Recall NumberZ-0577-2024
Recall Event ID 93507
510(K)NumberK173583 
Product Classification Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented - Product Code OQI
ProductAcuMatch Hip System, Catalog Number 142-32-27
Code Information GTIN 10885862538192, Serial Numbers: A673200, A673204, A673209
Recalling Firm/
Manufacturer		 Exactech, Inc.
2320 Nw 66th Ct
Gainesville FL 32653-1630
For Additional Information Contact
352-377-1140
Manufacturer Reason
for Recall		Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.
FDA Determined
Cause 2		Packaging change control
ActionExactech 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.
DistributionUS 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
Total Product Life CycleTPLC Device Report
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.
510(K) Database510(K)s with Product Code = OQI
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