RegWardenFDA facility compliance records
Company

ULRICH MEDICAL USA, INC.

3 recall(s) on record — most severe on record: Class II.

Recalls by year

FDA actions on record by year2017: 1 recalls; 2019: 2 recalls120172018220192020202120222023202420252026
  • Recalls (3)

Registered facilities (1)

Recalls & enforcement

  • Class IITerminated2019-12-31
    Due to a production error, the weld seam of the "Locking screw for crosslink, screw-to-screw" cannot reliably transmit the required torque of 3.5 Nm during installation.
  • Class IITerminated2019-03-08
    Certain Torque Limiting Handles in the field are beyond their 3 year calibration life.
  • Class IITerminated2017-03-07
    Surgical technique was revised to prevent static plate screws blocking mechanisms from disassociating.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.

Cite this record

RegWarden. “ULRICH MEDICAL USA, INC. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-9062154-ulrich-medical-usa-inc/

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