PlainRecalls

Medacta Usa Inc

Compiled from official public sources by the publisher.

17 recalls on record · Latest: Jul 8, 2026

Subscribe to new Medacta Usa Inc recalls (RSS)

Agency notice ledger

Federal filing book Medacta Usa Inc LIGHT-BOOK · SINGLE-AGENCY

#938 of 14,151 · 17 notices · 0.016% archive

  • BOOK 17 notices
  • RANK #938 of 14,151
  • SHARE 0.016% archive
  • AGENCY FDA Devices (17)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jul 8, 2026
  • PHOTO Actavis Inc

Nearest notice-volume peer: Actavis Inc (0 notice gap)

Medacta Usa Inc accounts for about 0.016% of the 104,423-notice archive on 17 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Medacta Usa Inc's standing among 14,151 recalling firms

Medacta Usa Inc ranks 938th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Medacta Usa Inc vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

17 938th of 14151 higher than 13,196 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Medacta Usa Inc in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Medacta Usa Inc holds about 0.016% of archive notices alongside 17 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jul 8, 2026

Short Monobloc Stem Broaches, Size/REF: 7/04.01.10.0970, 8/04.01.10.0971, 9/04.01.10.0972, 10/04.01.10.0973, 11/04.01.10.0974, 12/04.01.10.0975, 13/04.01.10.0976, 14/04.01.10.0977, 15/04.01.10.0978, 16/04.01.10.0979 Part of Medacta Shoulder System
FDA Devices Moderate Apr 26, 2023

MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device
FDA Devices Moderate Apr 26, 2023

MectaLIF ANTERIOR - Lag Plate Flush H14, REF 03.30.302, interbody fusion device
FDA Devices Moderate Apr 26, 2023

MectaLIF ANTERIOR - Antibackout Lag Cover, REF 03.30.305, interbody fusion device
FDA Devices Moderate Apr 26, 2023

MectaLIF ANTERIOR - Lag Plate Flush H18, REF 03.30.304, interbody fusion device
FDA Devices Moderate Apr 26, 2023

MectaLIF ANTERIOR - Lag Plate Flush H12, REF 03.30.301, interbody fusion device
FDA Devices Moderate Apr 26, 2023

MectaLIF ANTERIOR - Lag Plate Flush H16, REF 03.30.303, interbody fusion device
FDA Devices Moderate Dec 14, 2022

NextAR Shoulder Surgical Technique, Shoulder NextAR RSA Platform, CT based computer-assisted surgical navigation platform used to perform a reverse shoulder arthroplasty on the glenoid
FDA Devices Moderate Jun 15, 2022

GMK Efficiency - GMK Sphere CR Insert Instrument Set Size 1
FDA Devices Moderate Jan 15, 2020

Medacta Shoulder SYSTEM HUMERAL ANATOMICAL METAPHYSIS, REF 04.01.0023 through 04.01.0055, all sizes - Product Usage: The Medacta Anatomic Shoulder Prosthesis is indicated for treatment of humeral fractures and for primary or revision total shoulder replacement in patients with an intact or reparable rotator cuff shoulder joint, severe arthropathy or a previously failed joint replacement.
FDA Devices Moderate Oct 31, 2018

Medacta International MiniMAX CEMENTLESS ANATOMICAL STEM, 12/14: for cementless use in total or partial hip arthroplasty in primary or revision surgery.
FDA Devices Moderate Dec 27, 2017

The GMK knee system: designed for cemented use in total knee arthroplasty. Sphere and Primary Inserts with part number ranges: 02.12.0110FL - 02.12.0620FL; 02.12.0110FR - 02.12.0620FR; 02.07.0110PSF - 02.07.0620PSF
FDA Devices Moderate Jul 12, 2017

Medacta GMK HINGE, Tibial Insert Fixed, SIZE 2, HEIGHT 23 mm, REF 02.09.0223H, STERILE EO
FDA Devices Moderate Jan 25, 2017

Medacta International SA, M.U.S.T. Rod, REF 03.50.433, Size 5.5mm, Length 480mm, Type Straight, Mat Co-Cr-Mo The rods act as a connector between the different pedicle screws to create a stable construct for the stabilization and fusion of the lumbar and thoracic spine. Indications for Use: The M.U.S.T. pedicle screw system is intended for posterior non-cervical pedicle fixation (T1-S2/ilium) or anterolateral fixation (T8-L5). The pedicle screws are connected by 5.5mm Titanium alloy or CoCrM
FDA Devices Moderate Mar 6, 2013

Versafitcup Impacting Ring Model Number: 01.26.10.0133 (46mm), 01.26.10.0134 (48mm), 01.26.10.0135 (50mm), 01.26.10.0136 (52mm), 01.26.10.0137 (54mm), 01.26.10.0138 (56mm), 01.26.10.0139 (58mm), 01.26.10.0140 (60mm), 01.26.10.0141 (62mm), 01.26.10.0142 (64mm). Designed for cementless use in total hip arthroplasty.
FDA Devices Moderate Feb 13, 2013

Medacta Quadra Trial Broach size 0 part # 01.10.10.045, for use with the Medacta Total Hip Prosthesis System. Product Usage - used to broach the intramedullary canal of the femur in order to create space for the femoral stem during a hip replacement surgery.
FDA Devices Moderate Nov 14, 2012

Quadra S Offset Broach Handle The offset broach handle is intended to attach to the broaches of different sizes as the surgeon broaches the femoral bone in preparation for the implantation of the femoral stem.

Medacta Usa Inc holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Ad-Tech Medical Instrument Corporation 17 Fhc, Inc. 17 Ge Healthcare It 17 Hitachi Medical Systems America Inc 17

Frequently Asked Questions

How many federal recall notices name Medacta Usa Inc? ▼
PlainRecalls indexes 17 distinct federal recall events naming Medacta Usa Inc, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Medacta Usa Inc sit among other recalling firms? ▼
Medacta Usa Inc ranks #938 of 14,151 by distinct recall-event count among 14,151 firms in this archive (93rd percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Medacta Usa Inc's notices? ▼
FDA Devices accounts for 17 of this firm's 17 indexed notices.
What product category dominates Medacta Usa Inc's filing book? ▼
Filings for Medacta Usa Inc span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Medacta Usa Inc: 17 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Medacta Usa Inc; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026