# FDA recall Z-1725-2022

> **Exactech, Inc.** · Class II · device recall initiated 2022-08-11.

## Product

GXL acetabular liners, orthopedic hip implant component.  Product Line Numbers:    a. 0 DEG ACUMATCH CONSTRAINED LINER SZ E 28MM ID, REF 144-28-05;   b. 0 DEG ACUMATCH CONSTRAINED LINER SZ F 28MM ID, REF 144-28-06;   c. 0 DEG ACUMATCH CONSTRAINED LINER SZ G 28MM ID, REF 144-28-07;   d. 0 DEG ACUMATCH CONSTRAINED LINER SZ H 28MM ID, REF 144-28-08;   e. 0 DEG ACUMATCH CONSTRAINED LINER SZ J 28MM ID, REF 144-28-09;   f. 0 DEG ACUMATCH CONSTRAINED LINER SZ K 28MM ID, REF 144-28-10;   g. 0 DEG MCS CONSTRAINED LINER 50-52 MM, 28 MM ID, REF 146-28-04;   h. 0 DEG MCS CONSTRAINED LINER 54-58 MM, 28 MM ID, REF 146-28-05;   i. 0 DEG MCS CONSTRAINED LINER 60-64 MM, 32MM ID, REF 146-32-06;   j. O DEG ACUMATCH CONSTRAINED LINER SZ E 32MM ID, REF 144-32-05;   k. O DEG ACUMATCH CONSTRAINED LINER SZ F 32MM ID, REF 144-32-06;   l. O DEG ACUMATCH CONSTRAINED LINER SZ G 32MM ID, REF 144-32-07;   m. O DEG ACUMATCH CONSTRAINED LINER SZ H 32MM ID, REF 144-32-08;   n. O DEG ACUMATCH CONSTRAINED LINER SZ J 32M

## Reason for recall

Specific GXL acetabular polyethylene liners, packaged in non-conforming bags, may adversely impact the device and contribute to accelerated wear.

## Distribution

Worldwide distribution: US (nationwide) and OUS (foreign) countries of: ARGENTINA, BRAZIL, CHILE, CHINA, COLOMBIA, ECUADOR, GREECE, GUATEMALA, INDIA, LEBANON PORTUGAL,PUERTO RICO,SPAIN

## Key facts

- **Recall number:** Z-1725-2022
- **Recalling firm:** Exactech, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-08-11
- **Report date:** 2022-09-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Gainesville, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1725-2022

## Citation

> AI Analytics. FDA recall Z-1725-2022. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1725-2022. Source: US FDA. Licensed CC0.

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