--- title: "SPINEART SA Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search SPINEART SA recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/spineart-sa/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # SPINEART SA recall records **4** reported ongoing 4 records in this archive. Latest source date Jun 30, 2025. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. 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/). ## Records and reported status Jun 30, 2025 FDA device enforcement ### [Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Number: MPF-PS 65 40-S Software Version: Not Applicable Product Description: CANNUL...](https://isitonrecall.com/recall/fda-device-z-2279-2025-brand-name-perla-tl-mis-product-name-cannulated-fenestrated-polyaxial-screw-model-catalog-number-mpf/) Cannulated fenestrated polyaxial screws may be incorrectly labeled Class II Reported ongoing Distribution: US Nationwide distribution in the states of Florida , Kentucky, California. [Official source for Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Num...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2279-2025%22) Jun 30, 2025 FDA device enforcement ### [Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Number: MPF-PS 55 45-S Software Version: Not Applicable Product Description: CANNUL...](https://isitonrecall.com/recall/fda-device-z-2280-2025-brand-name-perla-tl-mis-product-name-cannulated-fenestrated-polyaxial-screw-model-catalog-number-mpf/) Cannulated fenestrated polyaxial screws may be incorrectly labeled Class II Reported ongoing Distribution: US Nationwide distribution in the states of Florida , Kentucky, California. [Official source for Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Num...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2280-2025%22) Mar 15, 2024 FDA device enforcement ### [PERLA TL 25D SCREW REF: TLF-DS 45 25-S TLF-DS 45 30-S TLF-DS 45 35-S TLF-DS 45 40-S TLF-DS 45 45-S TLF-DS 55 30-S TLF-DS 55 35-S TLF-DS 55 40-S TLF-DS 55 45-S TLF-DS 65 35-S TLF...](https://isitonrecall.com/recall/fda-device-z-1758-2024-perla-tl-25d-screw-ref-tlf-ds-45-25-s-tlf-ds-45-30-s-tlf-ds-45-35-s-tlf-ds-45-40-s-tlf-ds-45-45-s-tl/) Due to receiving information regarding difficulties with the insertion of a setscrew inside a screw head. Issues involved, either: 1. The setscrew is not tightened to torque 2. The setscrew is tightened to torque but position askew Class II Reported ongoing Distribution: U.S. Nationwide distribution in the states of CA, and KY. Not provided due to affected devices were manufactured O.U.S. [Official source for PERLA TL 25D SCREW REF: TLF-DS 45 25-S TLF-DS 45 30-S TLF-DS 45 35-S TLF-DS 45 40-S TLF-DS 45 45-...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1758-2024%22) Mar 16, 2023 FDA device enforcement ### [JULIET Ti LL, LATERAL LUMBAR TI-LIFE PLATE SMALL, REF: JLT-PL 02 08-S, JLT-PL 02 10-S, JLT-PL 02 12-S, JLT-PL 02 14-S, JLT-PL 02 16-S; JULIET Ti LL, LATERAL LUMBAR TI-LIFE PLATE...](https://isitonrecall.com/recall/fda-device-z-1426-2023-juliet-ti-ll-lateral-lumbar-ti-life-plate-small-ref-jlt-pl-02-08-s-jlt-pl-02-10-s-jlt-pl-02-12-s-jlt/) JULIET Lateral Lumbar Ti-Life Plate, a component of the JULIET Ti Lateral Lumbar Cage, may disassemble during the preparation stage before implantation, or during surgery when removing the implant holder, which could cause surgical delay. Class II Reported ongoing Distribution: US Nationwide distribution in the states of NH, TX, CA, VA, IL, RI, NC, AZ. [Official source for JULIET Ti LL, LATERAL LUMBAR TI-LIFE PLATE SMALL, REF: JLT-PL 02 08-S, JLT-PL 02 10-S, JLT-PL 02 ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1426-2023%22) ## Reasons in these listed records - Cannulated fenestrated polyaxial screws may be incorrectly labeled - Due to receiving information regarding difficulties with the insertion of a setscrew inside a screw head. Issues involved, either: 1. The setscrew is not tightened to torque 2. The setscrew is tightened to torque but position askew - JULIET Lateral Lumbar Ti-Life Plate, a component of the JULIET Ti Lateral Lumbar Cage, may disassemble during the preparation stage before implantation, or during surgery when removing the implant holder, which could cause surgical delay. These examples come from this result page and are not a ranking of every recall reason. ## Checking SPINEART SA ### Is there a recall on spineart sa right now? This archive contains 4 records, including 4 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search SPINEART SA](https://isitonrecall.com/check/?q=SPINEART%20SA) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)