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uCentum™ comprehensive posterior system CS 3802-075-035Recalls & reported problems

Ulrich GmbH & Co. KG · Screw, polyaxial, Ø 7.5 mm, length 35 mm perforated · Class 2 · Implant

All models of uCentum comprehensive posterior system (15)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04052536078875), received between Sep 29, 2016 and Sep 29, 2016 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (1 report).

1 other recall cover devices cleared under the same FDA submission (K123717); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Break1

Patient problems

  • Failure of Implant1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

Recalls under the same FDA submission

These recalls involve devices cleared under K123717. One submission often covers many models, so check the product and lot details in each record.

  • Z-1126-2019 · Mar 8, 2019 · Terminated
    ULRICH Torque Limiting Handle for use with a Set Screw Driver to perform the final tightening of set screws in a spinal implant construct.

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Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page