uCentumRecalls & reported problems across all models
Ulrich GmbH & Co. KG · 6 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 6
- Recalls
- 1
We found 6 models of uCentum by Ulrich GmbH & Co. KG in the FDA's device registry (GUDID). Together they are named in 7 adverse event reports in the FDA's MAUDE database, received between Aug 29, 2018 and Mar 25, 2026 — classified as 6 injuries, 1 malfunction.
The most frequently reported specific device problem is “Difficult to Remove” (4 reports).
1 FDA recall record name at least one of these models by its device identifier.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
uCentum recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Mar 8, 2019Terminated
Certain Torque Limiting Handles in the field are beyond their 3 year calibration life.
Z-1126-2019 · Root cause: Storage · names 2 of these models · Recall details · FDA record ↗
Most reported uCentum problems
Device problems
- Difficult to Remove4
- Material Separation3
- Fracture2
- Material Fragmentation1
- Physical Resistance/Sticking1
Patient problems
- No Known Impact Or Consequence To Patient4
- Foreign Body In Patient2
- No Clinical Signs, Symptoms or Conditions1
uCentum models
6 models, most reported first. Each model has its own page with its reports, recalls and device details.
- uCentum CS 7146Orthopedic Manual Surgical Instrument1 recall0 reports
- uCentum CS 7148Orthopedic Manual Surgical Instrument1 recall0 reports
- uCentum UL 8527-23Probe3 reports
- uCentum CS 3851-02Screwdriver2 reports
- uCentum CS 3020-01Thoracolumbosacral Pedicle Screw System1 report
- uCentum CS 7140Holder, Needle; Orthopedic1 report
Recent uCentum adverse event reports
The 7 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionMar 25, 2026Material Separation
INTRAOPERATIVE BREAKAGE OF A PEDICLE PROBE. IT WAS NOT POSSIBLE TO COMPLETE THE PLANNED PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24687488 ↗InjuryJul 9, 2019Fracture; Difficult to Remove; Fracture; Difficult to Remove
SURGEON DECIDED TO REMOVE SYSTEM AFTER FUSION HAD OCCURRED. WHEN REMOVING THE LOCKING SCREW THE SCREWDRIVER TIP BROKE OFF IN THE LOCKING SCREW AND COULD NOT BE REMOVED. THE SURGEON HAD TO DESTROY THE SCREW HEAD TO BE ABLE TO REMOVE THE SYSTEM.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8773544 ↗InjuryJul 9, 2019Fracture; Difficult to Remove; Fracture; Difficult to Remove
SURGEON DECIDED TO REMOVE SYSTEM AFTER FUSION HAD OCCURRED. WHEN REMOVING THE LOCKING SCREW THE SCREWDRIVER TIP BROKE OFF IN THE LOCKING SCREW AND COULD NOT BE REMOVED. THE SURGEON HAD TO DESTROY THE SCREW HEAD TO BE ABLE TO REMOVE THE SYSTEM.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8773541 ↗InjuryJun 28, 2019Difficult to Remove; Material Separation; Difficult to Remove; Material Separation
THE TIP OF A PROBE BROKE OFF DURING INSERTION INSIDE THE PATIENT. RETRIEVING THE TIP CAUSED APPROXIMATELY A ONE HOUR DELAY OF SURGERY. REPORT 2/2.
Patient problems: Foreign Body In Patient
MAUDE report 8745563 ↗InjuryJun 28, 2019Physical Resistance/Sticking; Physical Resistance/Sticking
THE SURGEON WAS NOT ABLE TO SUCCESSFULLY IMPLANT THE SCREW; TWO SCREWDRIVERS BROKE WHILE TRYING BUT REMAINED INTACT. HE DECIDED TO REMOVE THE SCREW AND BROKE ANOTHER SCREWDRIVER TRYING TO DO SO AND SEVERAL PIECES OF METAL BROKE OFF FROM THE SCREWDRIVER BUT WERE RECOVERED AND RETURNED ALONG WITH THE DRIVERS. THE SURGEON WAS ABLE TO REMOVE THE SCREW USING A ROD AND LOCKING SCREW. REPORT 5/5.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8745549 ↗InjuryNov 15, 2018Difficult to Remove; Material Separation; Difficult to Remove; Material Separation
THE TIP OF A PROBE BROKE OFF DURING INSERTION INSIDE THE PATIENT. RETRIEVING THE TIP CAUSED APPROXIMATELY A ONE HOUR DELAY OF SURGERY.
Patient problems: Foreign Body In Patient
MAUDE report 8073784 ↗InjuryAug 29, 2018Material Fragmentation; Material Fragmentation
THE SURGEON WAS NOT ABLE TO SUCCESSFULLY IMPLANT THE SCREW; TWO SCREWDRIVERS BROKE WHILE TRYING BUT REMAINED INTACT. HE DECIDED TO REMOVE THE SCREW AND BROKE ANOTHER SCREWDRIVER TRYING TO DO SO AND SEVERAL PIECES OF METAL BROKE OFF FROM THE SCREWDRIVER BUT WERE RECOVERED AND RETURNED ALONG WITH THE DRIVERS. THE SURGEON WAS ABLE TO REMOVE THE SCREW USING A ROD AND LOCKING SCREW.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7830276 ↗
Other Ulrich GmbH & Co. KG products
All Ulrich GmbH & Co. KG devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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