FDA Device recall Z-1726-2022

GXL acetabular liners, orthopedic hip implant component

FDA Device
Class II
ongoing
Published 2022-09-21

On 2022-09-21 the FDA classified a Class II recall of GXL acetabular liners, orthopedic hip implant component by Exactech, citing specific GXL acetabular polyethylene liners, packaged in non-conforming bags, may adversely impact the device and contribute to accelerated wear.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1726-2022
Classification	Class II
Status	ongoing
Initiated	2022-08-11
Published	2022-09-21
Last updated	2026-09-13 11:56 UTC
Company	Exactech
Distribution	US

Product

GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. ACUMATCH 15 DEGREE LINER 22MM SZ C, REF 132-22-03 b. ACUMATCH 15 DEGREE LINER 28MM SZ D, REF 13-28-04

Reason

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

Identifiers

code_info	a. REF 132-22-03, GUIDID 10885862022882, Serial Numbers: 1191262, 1191263, 1191264, 1191265, 1191266, 1191267, 1191268… a. REF 132-22-03, GUIDID 10885862022882, Serial Numbers: 1191262, 1191263, 1191264, 1191265, 1191266, 1191267, 1191268, 1191269, 1191270, 1191271, 1191272, 1191273, 1264678, 1264679, 1264680, 1264681, 1264682, 1264683, 1264685, 1264686, 1264687, 1264688, 1264689, 1264690, 1264691, 1264692, 1264693, 1264694, 1264695, 1264697, 1264698, 1264699, 1264700, 1264701, 1264703, 1264704, 1632156, 1632157, 1632158, 1632159, 1632160, 1632161, 1644095, 1644096, 1644097, 1644098, 1644099, 1644100, 1644101, 1644102, 1644103, 1644104, 1644105, 1644107, 1644108, 1644109, 1644111, 1644112, 1644113, 1644114, 2668582, 2668587, 2668594, 2668606; b. REF 13-28-04, GUDID 10885862022998, Serial Numbers: 569977, 569980, 569983, 569985, 569986, 569987, 569988, 569992, 617606, 617607, 617608, 617609, 617611, 617615, 617616, 617619, 617620, 705092, 705094, 705099, 705100, 705101, 705103, 705114, 705117, 766031, 766032, 766034, 766036, 766038, 774540, 774543, 774547, 774548, 774550, 774552, 774553, 774554, 77455

code_info

a. REF 132-22-03, GUIDID 10885862022882, Serial Numbers: 1191262, 1191263, 1191264, 1191265, 1191266, 1191267, 1191268…

a. REF 132-22-03, GUIDID 10885862022882, Serial Numbers: 1191262, 1191263, 1191264, 1191265, 1191266, 1191267, 1191268, 1191269, 1191270, 1191271, 1191272, 1191273, 1264678, 1264679, 1264680, 1264681, 1264682, 1264683, 1264685, 1264686, 1264687, 1264688, 1264689, 1264690, 1264691, 1264692, 1264693, 1264694, 1264695, 1264697, 1264698, 1264699, 1264700, 1264701, 1264703, 1264704, 1632156, 1632157, 1632158, 1632159, 1632160, 1632161, 1644095, 1644096, 1644097, 1644098, 1644099, 1644100, 1644101, 1644102, 1644103, 1644104, 1644105, 1644107, 1644108, 1644109, 1644111, 1644112, 1644113, 1644114, 2668582, 2668587, 2668594, 2668606; b. REF 13-28-04, GUDID 10885862022998, Serial Numbers: 569977, 569980, 569983, 569985, 569986, 569987, 569988, 569992, 617606, 617607, 617608, 617609, 617611, 617615, 617616, 617619, 617620, 705092, 705094, 705099, 705100, 705101, 705103, 705114, 705117, 766031, 766032, 766034, 766036, 766038, 774540, 774543, 774547, 774548, 774550, 774552, 774553, 774554, 77455

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1726-2022%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.