--- title: "GXL acetabular liners, orthopedic hip implant component. Product Line Numbers... — FDA record Z-1727-2022 | Is It on Recall" description: "Specific GXL acetabular polyethylene liners, packaged in non-conforming bags, may adversely impact the device and contribute to accelerated wear." url: https://isitonrecall.com/recall/fda-device-z-1727-2022-gxl-acetabular-liners-orthopedic-hip-implant-component-product-line-numbers-a-acumatch-5mm-lat-liner/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement # GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. ACUMATCH +5MM LAT LINER 15 DEG 36MM... — FDA record Z-1727-2022 Reported ongoing Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice. Source date Aug 11, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## What the record says - **Product**: GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. ACUMATCH +5MM LAT LINER 15 DEG 36MM ID, SIZE H, REF 138-36-08 b. ACUMATCH +5MM LAT LINER 15 DEG 36MM ID, SIZE J, REF 138-36-09 c. ACUMATCH LINER 15 DEG 36MM ID, SIZE H, REF 132-36-08 d. ACUMATCH LINER 15 DEG 36MM ID, SIZE J, REF 132-36-09 e. ACUMATCH LINER 15 DEG 36MM ID, SIZE K, REF 132-36-10 - **Reason**: Specific GXL acetabular polyethylene liners, packaged in non-conforming bags, may adversely impact the device and contribute to accelerated wear. - **Classification**: Class II - **Recalling firm**: Exactech, Inc. - **Quantity**: 132 devices - **Agency-reported status**: Ongoing - **Source record identifier**: Z-1727-2022 [Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1727-2022%22) [What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice. ## Lot and product identifiers | Label field | Details supplied by the agency | | --- | --- | | Lot, code or applicability | a. REF 138-36-08, GUDID 10885862024787, Serial Numbers: 638430, 638433, 638451, 638462, 638467; b. REF 138-36-09, GUDID 10885862024794, Serial Numbers: 635279, 635281; c. REF 132-36-08, GUDID 10885862023353, Serial Numbers: 630606, 630607, 630609, 630610, 630611, 630612, 630613, 632796, 632797, 632799, 632800, 632801, 632802, 632803, 632805, 632806, 632807, 632808, 632809, 632810, 632812, 632813, 632814, 632815, 632817, 632818, 632819, 632822, 632823, 632824, 632826, 632829, 632830, 632832, 632834, 657859, 657861, 657862, 657863, 657865, 657866, 657867, 657868, 657869, 657870, 657871, 657873, 657875, 657876, 657877, 657878, 657880, 657882, 657883, 657885, 657886, 657887, 657888, 657890, 657891, 657892, 1116881, 1116882, 1116883, 1116886, 1116887, 1116888, 1116889, 1116890, 1116892, 1116896, 1116897, 1116899, 1116903, 1116904, 1116905; d. REF 132-36-09, GUDID 10885862023360, Serial Numbers: 638946, 638947, 638950, 643861, 643862, 643863, 643864, 643865, 643866, 643867, 643868, 643869, 643870, 643871, 643872, 643874, 643876, 643877, 643878, 643879, 643880, 643881, 643882, 643883, 643884, 645796, 645798, 645799, 645800, 645801, 645802, 645803, 645805, 645806, 645807, 828079, 828082, 828083, 828084, 828085, 828086, 828088, 828089, 828090, 828091, 828092, 1634294, 2754889; e. REF 132-36-10, GUDID 10885862023377, Serial Numbers: 632861. | Match all identifying details in the current notice. A brand name alone is not enough. ## Distribution Worldwide distribution: US (nationwide) and OUS (foreign) countries of: ARGENTINA, BRAZIL, CHILE, CHINA, COLOMBIA, ECUADOR, GREECE, GUATEMALA, INDIA, LEBANON PORTUGAL,PUERTO RICO,SPAIN States below are derived from the distribution text, including nationwide wording. 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These dates are not interchangeable. ## What to do next Read the official notice for the action that applies to your exact product. [Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1727-2022%22) ## Related records [Medical devices records](https://isitonrecall.com/category/medical-devices/) [Exactech, Inc. records](https://isitonrecall.com/brand/exactech-inc/)