uCentum CS 7140Recalls & reported problems
Ulrich GmbH & Co. KG · T-handle with ratchet, coupling A · Class 1
All models of uCentum (6)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04052536078271), received between Jun 28, 2019 and Jun 28, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Physical Resistance/Sticking” (1 report).
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 16, 2026.
Most reported problems
Device problems
- Physical Resistance/Sticking1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
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 ↗
Other Holder, Needle; Orthopedic devices
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- Sklar® 96-2587Sklar Corporation · HOLDER, NEEDLE; ORTHOPEDIC1 recall0 reports
- Sklar Instruments 96-2358ASklar Corporation · HOLDER, NEEDLE; ORTHOPEDIC1 recall0 reports
- Sklar Instruments 96-2591ASklar Corporation · HOLDER, NEEDLE; ORTHOPEDIC1 recall0 reports
- Sklar Instruments 96-2583ASklar Corporation · HOLDER, NEEDLE; ORTHOPEDIC1 recall0 reports
- Sklar Instruments 96-2581Sklar Corporation · HOLDER, NEEDLE; ORTHOPEDIC1 recall0 reports
- Sklar Instruments 96-2585ASklar Corporation · HOLDER, NEEDLE; ORTHOPEDIC1 recall0 reports
- Sklar Instruments 96-2586Sklar Corporation · HOLDER, NEEDLE; ORTHOPEDIC1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- 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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