INHANCE 7505-10-105Recalls & reported problems
Depuy (Ireland) · INHANCE SHOULDER SYSTEM PERIPHERAL SCREW DRILL Ø3.2mm X 250mm · Class 1
All models of INHANCE (202)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295547679), received between Dec 12, 2022 and Oct 21, 2024 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Break” (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
- Break1
- Entrapment of Device1
Patient problems
- Insufficient Information1
- Unspecified Infection1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryOct 21, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED A PATIENT WAS REVISED ON (B)(6) 2024 DUE TO PROBABLE INFECTION. ORIGINAL IMPLANT DATE WAS (B)(6) 2023.
Patient problems: Unspecified Infection
MAUDE report 20498085 ↗MalfunctionDec 12, 2022Break; Entrapment of Device; Break; Entrapment of Device
IT WAS REPORTED THAT THE DRILL BIT TIP BROKE OFF IN THE LEFT SHOULDER.
Patient problems: Insufficient Information
MAUDE report 15958502 ↗
Other Instrument, surgical, orthopedic, dc-powered motor and accessory/attachment devices
- INHANCE 6505-10-103Depuy (Ireland) · Instrument, surgical, orthopedic, dc-powered motor and accessory/attachment209 reports
- INHANCE 6205-10-102Depuy (Ireland) · Instrument, surgical, orthopedic, dc-powered motor and accessory/attachment33 reports
- DELTA XTEND 2317-70-024Depuy (Ireland) · Instrument, surgical, orthopedic, dc-powered motor and accessory/attachment6 reports
- GLOBAL CAP 2230-81-110Depuy Orthopaedics, Inc. · Instrument, surgical, orthopedic, dc-powered motor and accessory/attachment5 reports
- INHANCE 6205-60-020Depuy (Ireland) · Instrument, surgical, orthopedic, dc-powered motor and accessory/attachment4 reports
- DELTA XTEND 2317-70-424Depuy (Ireland) · Instrument, surgical, orthopedic, dc-powered motor and accessory/attachment3 reports
- Stainless Steel Guide Wires 01-9473-3115Orthopediatrics Corp. · Instrument, surgical, orthopedic, dc-powered motor and accessory/attachment2 reports
- DELTA XTEND 2317-70-324Depuy (Ireland) · Instrument, surgical, orthopedic, dc-powered motor and accessory/attachment2 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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