DELTA XTEND 2307-92-003Recalls & reported problems
Depuy (Ireland) · DELTA Xtend LOCKING SCREWDRIVER MAIN BODY · Class 1
All models of DELTA XTEND (194)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This DePuy Delta Xtend locking screwdriver has 749 reports, with no deaths and 7 injuries. Most reports describe the screwdriver tip breaking, including during a shoulder replacement surgery. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 751
- Deaths reported
- 0
- Injuries reported
- 7
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 751 adverse event reports that list this exact device (DI 10603295116561), received between Jun 27, 2017 and Sep 18, 2026 — classified as 7 injuries, 744 malfunctions.
The most frequently reported specific device problem is “Break” (704 reports).
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.
Reports received per month
Most reported problems
Device problems
- Break704
- Material Deformation17
- Device-Device Incompatibility12
- Naturally Worn11
- Component Missing9
- Material Twisted/Bent7
- Entrapment of Device5
- Fracture5
Patient problems
- No Consequences Or Impact To Patient307
- No Clinical Signs, Symptoms or Conditions292
- Not Applicable59
- No Information58
- No Code Available30
- Insufficient Information29
- No Known Impact Or Consequence To Patient5
- Foreign Body In Patient2
Recent adverse event reports
The 25 most recent of 751 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 18, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50828523 ↗MalfunctionSep 14, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50754579 ↗MalfunctionAug 31, 2026Break
It was reported that during a Total Shoulder Replacement surgery the screwdriver tip broke. All available information has been disclosed.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50526489 ↗MalfunctionJul 27, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50038175 ↗MalfunctionJun 19, 2026Break
IT WAS REPORTED THAT THE DISTAL TIP OF LOCKING SCREWDRIVER WAS BROKEN ON THE PEG. THERE WAS NO HARM TO THE PATIENT. THERE WERE NO DELAYS TO THE PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25566377 ↗MalfunctionMar 4, 2026Break
IT WAS REPORTED TWO SCREW DRIVERS WERE BROKEN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24512139 ↗MalfunctionMar 4, 2026Break
IT WAS REPORTED TWO SCREW DRIVERS WERE BROKEN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24511664 ↗MalfunctionFeb 20, 2026Break
IT WAS REPORTED THAT THE SCREWDRIVER TIP WAS BROKEN. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24402460 ↗MalfunctionFeb 17, 2026Break
ONE OF THE TEETH AT THE END OF THE SCREWDRIVER SNAPPED OFF WHILE SURGEON WAS TIGHTENING ONE OF THE LOCKING SCREWS FIXING THE METAGLENE TO THE GLENOID. SURGEON WAS ABLE TO RETRIEVE THE BROKEN PIECE AND TIGHTEN THE SCREW SUFFICIENTLY. THE SURGERY TIME WAS DELAYED BRIEFLY BUT THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24366921 ↗MalfunctionFeb 2, 2026Break
IT WAS REPORTED THAT LOCKING SCREWDRIVER TIME BROKE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24238968 ↗MalfunctionJan 27, 2026Break
IT WAS REPORTED THAT DURING AN ARTHROPLASTY SURGICAL PROCEDURE, THE DELTA XTEND LOCKING SCREWDRIVER TINE SNAPPED WHEN INSERTING LOCKING SCREW INTO METAGLENE. WAS SURGERY DELAYED DUE TO THE REPORTED EVENT? NO, ACTION TAKEN WHEN EVENT OCCURRED? REPLACE WITH SPARE SCREWDRIVER, WAS PROCEDURE SUCCESSFULLY COMPLETED? YES, WERE FRAGMENTS GENERATED? YES, IF YES, WERE THEY REMOVED EASILY WITHOUT ADDITIONAL INTERVENTION? YES, PATIENT STATUS/ OUTCOME / CONSEQUENCES NO, WAS OTHER MEDICAL INTERVENTION (E.G. X-RAYS, ADDITIONAL PROCEDURES, PRESCRIPTIONS, OTC, REVISION) REQUIRED: UNKNOWN, IS THE PATIENT PART OF A CLINICAL STUDY UNKNOWN,
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24190091 ↗MalfunctionJan 23, 2026Break
IT WAS REPORTED THAT THE TOOTH BROKE OFF OF THE SCREWDRIVER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24159697 ↗MalfunctionJan 5, 2026Break
IT WAS REPORTED THAT DURING AN ORTHOPEDIC PROCEDURE THE SCREWDRIVER BROKE AND THERE WERE NO PATIENT CONSEQUENCES OR REPORTED HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23963409 ↗MalfunctionDec 18, 2025Break; Break
IT WAS REPORTED THAT THERE WAS A TYNE BROKE ON THE SCREWDRIVER DURING NORMAL USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23837935 ↗MalfunctionDec 3, 2025Break; Break
IT WAS REPORTED THAT TYNE BROKE OFF DELTA LOCKING SCREW DRIVER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23704259 ↗MalfunctionNov 17, 2025Break; Break
IT WAS REPORTED THAT ONE OF THE PRONGS ON THE GREEN SCREWDRIVER BROKE DURING WASHING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23572101 ↗MalfunctionNov 6, 2025Break; Break
IT WAS REPORTED THAT THAT THE INSTRUMENT BROKE WHILE SURGEON WAS USING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23491280 ↗MalfunctionSep 17, 2025Break; Break
IT WAS REPORTED THAT THE INSTRUMENT IS BROKEN & NEEDS TO BE REPLACED. IT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23075509 ↗MalfunctionSep 9, 2025Break; Break
IT WAS REPORTED THE TIP OF THE SCREWDRIVER WAS DAMAGED. THIS WAS IDENTIFIED DURING LOAN KIT INSPECTION. THERE WAS NO PATIENT OR PROCEDURE INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23008560 ↗MalfunctionJul 23, 2025Break; Break
IT WAS REPORTED THAT THE PRONG OF LOCKING SCREW DRIVER BROKE OFF IN PATIENT. THIS WAS A CONSIGNED KIT. AN X-RAY WAS TAKEN TO FIND THE MISSING PRONG. THERE WAS A SURGICAL DELAY. AN ALTERNATIVE INSTRUMENT WAS USED TO SUCCESSFULLY COMPLETE THE PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22576422 ↗MalfunctionJul 1, 2025Break; Break
IT WAS REPORTED THAT THE ATTUNE FEMORAL IMPACTOR WAS ONE CRACK AWAY FROM BREAKING. PINN GB OFFSET GRATER HANDLE WAS SEPARATED. QUICKSET ACE GRATER HANDLE WAS TOUGH TO PULL DOWN. QUICKSET ACE GRATER HEAD 51MM WAS DULL. LOCKING SCREWDRIVER BODY HAD PART OF TOP METAL BROKEN. THE EVENTS DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22370412 ↗MalfunctionJun 24, 2025Break; Break
IT WAS REPORTED THAT SPLINE OF LOCKING SCREWDRIVER BROKE WHILE SCREWING IN BASEPLATE SCREW. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED FOR REPORTING. NO FURTHER INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22323597 ↗MalfunctionJun 23, 2025Break; Break
IT WAS REPORTED THAT THE SCREWDRIVER PRONG WAS BROKEN. ONLY ONE OF THE 4 PRONGS BROKE SO DEVICE WAS IN 2 PIECES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22307079 ↗MalfunctionJun 13, 2025Break; Break
IT WAS REPORTED THAT THIS WAS J&J STAFF TRAINING AT THE J&J K.K. ON (B)(6) 2025. IN THE TRAINING, DURING A TREATMENT ON THE GLENOID SIDE, A LOCKING SCREWDRIVER WAS USED TO FIX THE METAGLEN WITH A LOCKING SCREW, BUT THE NAIL AT THE TIP BROKE (CHIPPED OFF). THE SCREW WAS TIGHTENED WITH THE GROOVES PROPERLY INTERLOCKING (THE CONVEX AND CONCAVE PARTS WERE PROPERLY ENGAGED). NO ACTUAL HARM WAS CAUSED TO PATIENTS DURING STAFF TRAINING. NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22204418 ↗MalfunctionMay 30, 2025Break; Break
THE SCREWDRIVER HAS BEEN IDENTIFIED WITH BROKEN ¿PRONGS¿ AT THE TIP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22114863 ↗
Other SCREWDRIVER devices
- EXPEDIUM 279712400Medos International Sàrl · SCREWDRIVER551 reports
- NA 314.467Synthes GmbH · SCREWDRIVER498 reports
- N/A 5584111Medtronic Sofamor Danek, Inc. · SCREWDRIVER492 reports
- QUICKSET 2274-47-000Depuy (Ireland) · SCREWDRIVER487 reports
- NA 03.130.010Synthes GmbH · SCREWDRIVER1 recall422 reports
- QUICKSET 2274-63-000Depuy (Ireland) · SCREWDRIVER404 reports
- EVOS 71175072Smith & Nephew, Inc. · SCREWDRIVER336 reports
- NA 2274-02-000Depuy (Ireland) · SCREWDRIVER303 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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