DJO SURGICAL 804-06-332Recalls & reported problems
Encore Medical, L.P. · AltiVate Reverse Glenoid Peripheral Screw T20 Driver · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00190446844198), received between Mar 21, 2025 and Apr 13, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Detachment of Device or Device Component1
- No Apparent Adverse Event1
Patient problems
- Foreign Body In Patient2
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 13, 2026No Apparent Adverse Event
THE SURGEON HAD THE T20 TORX DRIVER ON POWER AND WAS USING THAT TO SCREW THE SCREW INTO THE BASEPLATE. WHEN THE SURGEON DID THAT, THE TIP OF THE TORX DRIVER SHEARED OFF INTO THE SCREW.
Patient problems: Foreign Body In Patient
MAUDE report 24864583 ↗MalfunctionFeb 2, 2026Detachment of Device or Device Component
INSTRUMENT FAILURE - TORX BIT TIP BROKE OFF INSIDE PATIENT AND COLD WELDED TO SCREW. SURGEON WAS UNABLE TO REMOVE BROKEN TIP FROM SCREW. TIP WAS LEFT IN PATIENT.
Patient problems: Foreign Body In Patient
MAUDE report 24242452 ↗MalfunctionMar 21, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
INSTRUMENT FAILURE - INSTRUMENT FAILURE, FRAGMENTS LEFT IN PATIENT
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21670662 ↗
Other SCREWDRIVER devices
- DELTA XTEND 2307-92-003Depuy (Ireland) · SCREWDRIVER751 reports
- 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
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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