# FDA recall Z-1734-2022

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

## Product

GXL acetabular liners, orthopedic hip implant component.  Product Line Numbers:    a. ACUMATCH 0 DEGREE LINER 28MM 46MM, REF 130-28-05;   b. ACUMATCH 0 DEGREE LINER 28MM 48MM, REF 130-28-06;   c. ACUMATCH 0 DEGREE LINER 28MM 50/52MM, REF 130-28-07;   d. ACUMATCH 0 DEGREE LINER 28MM 54/56MM, REF 130-28-08;   e. ACUMATCH 0 DEGREE LINER 28MM 58/64MM, REF 130-28-09;   f. ACUMATCH 15 DEGREE LINER 22MM SZ D, REF 132-22-04;   g. ACUMATCH 15 DEGREE LINER 22MM SZ E, REF 132-22-05;   h. ACUMATCH 15 DEGREE LINER 22MM SZ F, REF 132-22-06;   i. ACUMATCH 15 DEGREE LINER 22MM  SZ G, REF 132-22-07;   j. ACUMATCH 15 DEGREE LINER 22MM   SZ H, REF 132-22-08;   k. ACUMATCH 15 DEGREE LINER 28MM SZ E, REF 132-28-05;   l. ACUMATCH 15 DEGREE LINER 28MM SZ F, REF 132-28-06;   m. ACUMATCH 15 DEGREE LINER 28MM SZ G, REF 132-28-07;   n. ACUMATCH 15 DEGREE LINER 28MM SZ H, REF 132-28-08;   o. ACUMATCH 15 DEGREE LINER 28MM SZ J, REF 132-28-09;   p. ACUMATCH 15 DEGREE LINER 28MM SZ K, REF 132-28-10;   q. ACUMATCH 15

## 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-1734-2022
- **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-1734-2022

## Citation

> AI Analytics. FDA recall Z-1734-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1734-2022. Source: US FDA. Licensed CC0.

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