Recall Register

Device recall: AcuMatch Hip System, Catalog Number 142-32-27

Class II FDA enforcement event 93507. Recall start date: . Status in the FDA record: Ongoing.

Reason for recall, in the words of FDA

Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

Exactech, Inc. started this device recall on 21 Nov 2023. The firm address in the FDA record is in Gainesville, FL. FDA put the recall in Class II. FDA event 93507 has 12 product records. The first FDA enforcement report date is 27 Dec 2023. The record gives the status Ongoing.

FDA enforcement reportThe 12 product records

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

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

Recalling firm

Exactech, Inc., Gainesville, FL.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

12 product records in the event.

FDA event 93507: product records
Recall numberProductQuantityClassStatusReport date
Z-0577-2024AcuMatch Hip System, Catalog Number 142-32-27N/AClass IIOngoing27 Dec 2023
Z-0578-2024Exactech Alteon Hip XLE Liner, Catalog Numbers: a) 01-030-40-0636, b) 01-030-40-0640, c) 01-030-42-0536N/AClass IIOngoing27 Dec 2023
Z-0579-2024Exactech Equinoxe Reverse Shoulder System, Catalog Numbers: a) 320-36-00, b) 320-36-03, c) 320-36-04, d) 320-36-10, e) 320-36-13, f) 320-38-00, g) 320-38-13, h) 320-40-00, i) 320-40-10, j) 320-42-00, k) 320-42-10, l) 320-42-13, m) 320-46-10, n) 320-46-13N/AClass IIOngoing27 Dec 2023
Z-0580-2024Exactech Equinoxe Shoulder System, Catalog Numbers: a) 314-23-02, b) 314-23-03, c) 314-23-13, d) 314-23-14, e) 314-23-15, f) 314-24-22, g) 314-24-23, h) 314-24-24, i) 314-24-32, j) 314-24-33, k) 314-24-34, l) 314-24-35N/AClass IIOngoing27 Dec 2023
Z-0581-2024Exactech Novation Hip System, Catalog Numbers: 134-36-45N/AClass IIOngoing27 Dec 2023
Z-0582-2024Exactech Optetrak Knee System, Catalog Numbers: a) 200-02-26, b) 200-02-29, c) 200-02-32, d) 200-02-35, e) 200-02-38, f) 200-02-41, g) 200-03-32, h) 200-07-29, i) 200-07-32, j) 200-07-35, k) 204-21-13, l) 204-22-26, m) 208-23-18, n) 208-24-13N/AClass IIOngoing27 Dec 2023
Z-0583-2024Exactech Optetrak Logic Knee System, Catalog Numbers: a) 02-012-47-3011, b) 02-012-47-5009, c) 02-012-47-5011, d) 02-012-65-3013N/AClass IIOngoing27 Dec 2023
Z-0584-2024Exactech Optetrak Logic PS Knee System, Catalog Numbers: 02-012-35-5009N/AClass IIOngoing27 Dec 2023
Z-0585-2024Exactech Truliant Knee System, Catalog Numbers: a) 02-012-35-3509, b) 02-022-35-1509, c) 02-022-35-1513, d) 02-022-35-3010, e) 02-022-35-3509, f) 02-022-35-3510, g) 02-022-35-3511, h) 02-022-35-4511, i) 02-022-44-3512, j) 02-022-47-2509, k) 02-022-51-4519N/AClass IIOngoing27 Dec 2023
Z-0586-2024Exactech Truliant, Activit-E Knee Insert, Catalog Numbers: a) 02-023-02-0029, b) 02-023-02-0032, c) 02-023-02-0035, d) 02-023-02-0038, e) 02-024-35-1512, f) 02-024-35-1515, g) 02-024-35-1519, h) 02-024-35-2010, i) 02-024-35-2013, j) 02-024-35-2015, k) 02-024-35-2509, l) 02-024-35-2510, m) 02-024-35-2511, n)…N/AClass IIOngoing27 Dec 2023
Z-0587-2024Exactech Vantage Ankle System, Catalog Numbers: a) 350-21-04, b) 350-22-03N/AClass IIOngoing27 Dec 2023
Z-0588-2024Exactech Vantage Mobile Bearing Tibial Inserts, Catalog Numbers: a) 350-41-23, b) 350-42-03N/AClass IIOngoing27 Dec 2023

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class II: The middle of the three FDA recall classes.

The event in context

Device events that started in 2023
917
Share of these events in Class II
88%
Product records in this event
12Median of the firm: 1
Events of the firm on the register
61

Other events of the firm

Other FDA enforcement events of Exactech, Inc.
InitiatedProduct (first record)TypeClassRecords
3 Feb 2026Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog Number: 321-09-05DeviceClass II2
5 Sep 2025Brand Name: Equinoxe Ergo Product Name: Adjustable Angle rTSA Reamer, 42mm Model/Catalog Number: 321-59-42 Software VersDeviceClass II3
15 Aug 2025Exactech Equinoxe, Reverse Shoulder Humeral Liners, REF: 320-38-00,145-DEG PE 38MM HUM LINER +0/ 320-38-03,145-DEG PE 38DeviceClass II2
31 Dec 2024AcuMatch XLE Item Number / Product Description: 140-28-27 AM EHXL 0¿ LNR G 28MM 140-32-27 AM EHXL 0¿ LNR G 32MM 140-32-2DeviceClass II3
26 Apr 2024Acumatch L-Series BIPOLAR LINER, 22mm (BIPOLAR ENDOPROSTHESIS-Hip), Item Numbers: a) 100-22-19, SZ. L; b) 100-22-20, SZ.DeviceClass II1
18 Apr 2024OPTETRAK Three Peg Patella, Item Numbers: a) 200-02-26, 26MM; b) 200-02-29, 29MM; c) 200-02-32, 32MM; d) 200-02-35, 35MMDeviceClass II4
6 Mar 2024Exactech Equinoxe GLENOID,KEELED, CEMENTED, Mates with 38, 41, 44 head, alpha curvature, Sizes: a), Small, Item Number 3DeviceClass II24
5 Jun 2023Exactech Shoulder GPS Impactor Handle, Catalog #531-07-05.DeviceClass II2
11 Aug 2022GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. 0 DEG ACUMATCH CONSTRAINED LINER SZ E DeviceClass II10
30 Aug 2021OPTETRAK Comprehensive Knee System, labeled as the following: a. OPTETRAK All-polyethylene CR Tibial Components, with PrDeviceClass II9

Exactech, Inc.: all 61 events

Official channels

Cite this page

Recall Register. FDA enforcement event 93507. https://recallregister.com/fda/ii/93507/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA device enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this 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
What quantity of product is in FDA event 93507?
The event has 12 product records. The first record gives this quantity: N/A
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many device recalls of 2023 have the same class?
88% of the 917 device events that started in 2023 are in Class II.