--- title: "MicroPort Orthopedics Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search MicroPort Orthopedics Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/microport-orthopedics-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # MicroPort Orthopedics Inc. recall records **3** reported ongoing 6 records in this archive. Latest source date Dec 19, 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 Dec 19, 2025 FDA device enforcement ### [Brand Name: MicroPort Product Name: HIPTURN FEM HEAD TRIAL 36MM REUSABLE Model/Catalog Number: HTHT0036 Software Version: N/A Product Description: HIPTURN FEM HEAD TRIAL 36MM RE...](https://isitonrecall.com/recall/fda-device-z-1133-2026-brand-name-microport-product-name-hipturn-fem-head-trial-36mm-reusable-model-catalog-number-htht0036/) Due to products not having FDA Premarket authorization to be distributed within the United States. Class II Reported ongoing Distribution: The product was sent to distributors in multiple US states, including Texas, California, Wisconsin, Kansas, Illinois, Michigan, Tennessee, Maryland, Washington, Georgia, Colorad... [Official source for Brand Name: MicroPort Product Name: HIPTURN FEM HEAD TRIAL 36MM REUSABLE Model/Catalog Number: HT...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1133-2026%22) Oct 29, 2024 FDA device enforcement ### [EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; EVOLUTION MP FEMORAL COMPONENT CS/CR NON-POROUS SIZE 6 LEFT PRIMARY, REF: EFSRN6PL Knee prosthes...](https://isitonrecall.com/recall/fda-device-z-0699-2025-evolution-mp-femoral-component-cs-cr-porous-size-5-right-primary-ref-efsrp5pr-evolution-mp-femoral-c/) Femoral implant porous size 5 right primary and femoral implant non-porous size 6 left primary have correct markings on devices, but may have incorrect packaging. Class II Reported ongoing Distribution: OUS: CN, GR, ES, ZA, FR, JP, IT [Official source for EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; EVOLUTION MP FEM...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0699-2025%22) May 3, 2024 FDA device enforcement ### [EVOLUTION¿ MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee replacement implants are for cemented use only.](https://isitonrecall.com/recall/fda-device-z-2244-2024-evolution-mp-femoral-cs-cr-non-porous-non-porous-microport-total-knee-replacement-implants-are-for-c/) One confirmed incident has been received that EFSRN4PR, lot number MP1982170, Size 4 Evolution MP Non-Porous Femoral Right was opened during surgery and contained part number EFSRN3PL, lot number MP1982097, Size 3 Evolution MP Non-Porous Femoral Left in the... Class II Reported ongoing Distribution: International distribution in the country of China. There is no field inventory in the United States for either lot. [Official source for EVOLUTION¿ MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee replacement implants are f...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2244-2024%22) Oct 28, 2022 FDA device enforcement ### [EVOLUTION MP Tibial Bases, Size 2+ LEFT, REF ETPKN2PL, knee tibial base](https://isitonrecall.com/recall/fda-device-z-0275-2023-evolution-mp-tibial-bases-size-2-left-ref-etpkn2pl-knee-tibial-base/) One confirmed incident has been received that ETPKN2PL lot 1916559, size 2 Evolution MP Tibial Base, was opened during surgery and contained ETPKN7SL lot 1916715, size 7 Evolution MP Tibial Base, in the packaging. Class II Reported terminated Distribution: International Distribution to countries of: Germany, Italy, France, Belgium, Austria, Greece, Romania, Japan, and P.R. China. [Official source for EVOLUTION MP Tibial Bases, Size 2+ LEFT, REF ETPKN2PL, knee tibial base](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0275-2023%22) Oct 28, 2022 FDA device enforcement ### [EVOLUTION MP Tibial Bases, Size 7 LEFT, REF ETPKN7SL, knee tibial base](https://isitonrecall.com/recall/fda-device-z-0276-2023-evolution-mp-tibial-bases-size-7-left-ref-etpkn7sl-knee-tibial-base/) One confirmed incident has been received that ETPKN2PL lot 1916559, size 2 Evolution MP Tibial Base, was opened during surgery and contained ETPKN7SL lot 1916715, size 7 Evolution MP Tibial Base, in the packaging. Class II Reported terminated Distribution: International Distribution to countries of: Germany, Italy, France, Belgium, Austria, Greece, Romania, Japan, and P.R. China. [Official source for EVOLUTION MP Tibial Bases, Size 7 LEFT, REF ETPKN7SL, knee tibial base](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0276-2023%22) May 4, 2022 FDA device enforcement ### [PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK](https://isitonrecall.com/recall/fda-device-z-1225-2022-profemur-plasma-z-classic-stem-size-7-standard-short-neck/) One manufacturing lot is missing the plasma-spray coating in the proximal region of the stem body. Class II Reported terminated Distribution: Worldwide distribution - US Nationwide distribution in the states of FL, IN, MO, CA and the country of Canada. [Official source for PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1225-2022%22) ## Reasons in these listed records - Due to products not having FDA Premarket authorization to be distributed within the United States. - Femoral implant porous size 5 right primary and femoral implant non-porous size 6 left primary have correct markings on devices, but may have incorrect packaging. - One confirmed incident has been received that EFSRN4PR, lot number MP1982170, Size 4 Evolution MP Non-Porous Femoral Right was opened during surgery and contained part number EFSRN3PL, lot number MP1982097, Size 3 Evolution MP Non-Porous Femoral Left in the packaging. - One confirmed incident has been received that ETPKN2PL lot 1916559, size 2 Evolution MP Tibial Base, was opened during surgery and contained ETPKN7SL lot 1916715, size 7 Evolution MP Tibial Base, in the packaging. These examples come from this result page and are not a ranking of every recall reason. ## Checking MicroPort Orthopedics Inc. ### Is there a recall on microport orthopedics inc. right now? This archive contains 6 records, including 3 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 MicroPort Orthopedics Inc.](https://isitonrecall.com/check/?q=MicroPort%20Orthopedics%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)