--- title: "Medacta Usa Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Medacta Usa 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/medacta-usa-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Medacta Usa Inc recall records **1** reported ongoing 9 records in this archive. Latest source date Apr 30, 2026. 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 Apr 30, 2026 FDA device enforcement ### [Short Monobloc Stem Broaches, Size/REF: 7/04.01.10.0970, 8/04.01.10.0971, 9/04.01.10.0972, 10/04.01.10.0973, 11/04.01.10.0974, 12/04.01.10.0975, 13/04.01.10.0976, 14/04.01.10.09...](https://isitonrecall.com/recall/fda-device-z-2618-2026-short-monobloc-stem-broaches-size-ref-7-04-01-10-0970-8-04-01-10-0971-9-04-01-10-0972-10-04-01-10-09/) Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming guide and the stem reamer are positioned approximately 0.2 mm per size more laterally than intended, which may i... Class II Reported ongoing Distribution: US Nationwide distribution in the states of CO, AR, IN, PA, UT, FL. [Official source for Short Monobloc Stem Broaches, Size/REF: 7/04.01.10.0970, 8/04.01.10.0971, 9/04.01.10.0972, 10/04....](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2618-2026%22) Mar 8, 2023 FDA device enforcement ### [MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device](https://isitonrecall.com/recall/fda-device-z-1400-2023-mectalif-anterior-lag-plate-flush-h10-ref-03-30-300-interbody-fusion-device/) There is a potential for breakage of the small screw used to affix the anti-backout plate. Class II Reported completed Distribution: US: ID, TX, GA, VA, AZ [Official source for MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1400-2023%22) Mar 8, 2023 FDA device enforcement ### [MectaLIF ANTERIOR - Lag Plate Flush H12, REF 03.30.301, interbody fusion device](https://isitonrecall.com/recall/fda-device-z-1401-2023-mectalif-anterior-lag-plate-flush-h12-ref-03-30-301-interbody-fusion-device/) There is a potential for breakage of the small screw used to affix the anti-backout plate. Class II Reported completed Distribution: US: ID, TX, GA, VA, AZ [Official source for MectaLIF ANTERIOR - Lag Plate Flush H12, REF 03.30.301, interbody fusion device](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1401-2023%22) Mar 8, 2023 FDA device enforcement ### [MectaLIF ANTERIOR - Lag Plate Flush H14, REF 03.30.302, interbody fusion device](https://isitonrecall.com/recall/fda-device-z-1402-2023-mectalif-anterior-lag-plate-flush-h14-ref-03-30-302-interbody-fusion-device/) There is a potential for breakage of the small screw used to affix the anti-backout plate. Class II Reported completed Distribution: US: ID, TX, GA, VA, AZ [Official source for MectaLIF ANTERIOR - Lag Plate Flush H14, REF 03.30.302, interbody fusion device](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1402-2023%22) Mar 8, 2023 FDA device enforcement ### [MectaLIF ANTERIOR - Lag Plate Flush H16, REF 03.30.303, interbody fusion device](https://isitonrecall.com/recall/fda-device-z-1403-2023-mectalif-anterior-lag-plate-flush-h16-ref-03-30-303-interbody-fusion-device/) There is a potential for breakage of the small screw used to affix the anti-backout plate. Class II Reported completed Distribution: US: ID, TX, GA, VA, AZ [Official source for MectaLIF ANTERIOR - Lag Plate Flush H16, REF 03.30.303, interbody fusion device](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1403-2023%22) Mar 8, 2023 FDA device enforcement ### [MectaLIF ANTERIOR - Lag Plate Flush H18, REF 03.30.304, interbody fusion device](https://isitonrecall.com/recall/fda-device-z-1404-2023-mectalif-anterior-lag-plate-flush-h18-ref-03-30-304-interbody-fusion-device/) There is a potential for breakage of the small screw used to affix the anti-backout plate. Class II Reported completed Distribution: US: ID, TX, GA, VA, AZ [Official source for MectaLIF ANTERIOR - Lag Plate Flush H18, REF 03.30.304, interbody fusion device](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1404-2023%22) Mar 8, 2023 FDA device enforcement ### [MectaLIF ANTERIOR - Antibackout Lag Cover, REF 03.30.305, interbody fusion device](https://isitonrecall.com/recall/fda-device-z-1405-2023-mectalif-anterior-antibackout-lag-cover-ref-03-30-305-interbody-fusion-device/) There is a potential for breakage of the small screw used to affix the anti-backout plate. Class II Reported completed Distribution: US: ID, TX, GA, VA, AZ [Official source for MectaLIF ANTERIOR - Antibackout Lag Cover, REF 03.30.305, interbody fusion device](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1405-2023%22) Oct 27, 2022 FDA device enforcement ### [NextAR Shoulder Surgical Technique, Shoulder NextAR RSA Platform, CT based computer-assisted surgical navigation platform used to perform a reverse shoulder arthroplasty on the ...](https://isitonrecall.com/recall/fda-device-z-0372-2023-nextar-shoulder-surgical-technique-shoulder-nextar-rsa-platform-ct-based-computer-assisted-surgical/) A warning has been added to the Surgical Technique for NextAR Shoulder, advising verification of suitable patient conditions prior to placement of the NextAR Shoulder Target Holder: WARNING Target fixation requires adequate coracoid bone stability. Osteopor... Class II Reported terminated Distribution: AL, FL, NH, CO, IL, SC, AR [Official source for NextAR Shoulder Surgical Technique, Shoulder NextAR RSA Platform, CT based computer-assisted surg...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0372-2023%22) Apr 13, 2022 FDA device enforcement ### [GMK Efficiency - GMK Sphere CR Insert Instrument Set Size 1](https://isitonrecall.com/recall/fda-device-z-1247-2022-gmk-efficiency-gmk-sphere-cr-insert-instrument-set-size-1/) A Size 2 trial baseplate was assembled with Size 1 instrument sets. Class II Reported terminated Distribution: Distribution was made to AK, CA, CT, IN, MA, NJ, and PA. There was no foreign/military/government distribution. [Official source for GMK Efficiency - GMK Sphere CR Insert Instrument Set Size 1](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1247-2022%22) ## Reasons in these listed records - Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming guide and the stem reamer are positioned approximately 0.2 mm per size more laterally than intended, which may increase the risk of ... - There is a potential for breakage of the small screw used to affix the anti-backout plate. - A warning has been added to the Surgical Technique for NextAR Shoulder, advising verification of suitable patient conditions prior to placement of the NextAR Shoulder Target Holder: WARNING Target fixation requires adequate coracoid bone stability. Osteoporosis, weakness of th... - A Size 2 trial baseplate was assembled with Size 1 instrument sets. These examples come from this result page and are not a ranking of every recall reason. ## Checking Medacta Usa Inc ### Is there a recall on medacta usa inc right now? This archive contains 9 records, including 1 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 Medacta Usa Inc](https://isitonrecall.com/check/?q=Medacta%20Usa%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)