PlainRecalls

Medacta Usa Inc

Compiled from official public sources by the editorial team.

16 recalls on record · Latest: Apr 26, 2023

Medacta Usa Inc Recall Insight

Medacta Usa Inc appears on 16 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.016% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Apr 26, 2023, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 16 entries, severity tagging shows 0 critical, 16 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 16 of 16 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (16). The date window on this page runs from Nov 14, 2012 to Apr 26, 2023.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

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 s…

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 Pr…

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 surge…

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…

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…

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 (54…

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 …

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 femora…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.