Medacta recalls

4 official recalls and safety alerts involving Medacta since 2022-06, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.

This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Medacta or the relevant agency.

  1. 2026-07-08
  2. US
    Drugs & medicalClass II

    Medacta Usa Inc recalls 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,…

    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…

    FDA · DeviceMedacta Usa IncUS Nationwide distribution in the states of CO, AR, IN, PA, UT, FL.Official notice →
  3. 2023-04-26
  4. US
    Drugs & medicalClass II

    Medacta Usa Inc recalls 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.

    FDA · DeviceMedacta Usa IncUS: ID, TX, GA, VA, AZOfficial notice →
  5. 2022-12-14
  6. US
    Drugs & medicalClass II

    Medacta Usa Inc recalls NextAR Shoulder Surgical Technique, Shoulder NextAR RSA Platform, CT based computer-assisted surgical navigation platform used to perform…

    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…

    FDA · DeviceMedacta Usa IncAL, FL, NH, CO, IL, SC, AROfficial notice →
  7. 2022-06-15
  8. US
    Drugs & medicalClass II

    Medacta Usa Inc recalls GMK Efficiency - GMK Sphere CR Insert Instrument Set Size 1

    A Size 2 trial baseplate was assembled with Size 1 instrument sets.

    FDA · DeviceMedacta Usa IncDistribution was made to AK, CA, CT, IN, MA, NJ, and PA. There was no…Official notice →