Arthrex® AR-8750-05Recalls & reported problems

Arthrex, Inc. · PRFL DRL, 5.0MM CMPR FT · Class 1

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 00888867263703), received between Aug 11, 2023 and Aug 11, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Overheating of Device” (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

Overheating of Device1

Patient problems

Full thickness (Third Degree) Burn1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

InjuryAug 11, 2023Overheating of Device; Overheating of Device
ON (B)(6) 2023, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA SEMS THAT AN AR-8750-05 PROFILE DRILL WAS OVERHEATING AND BURNING BONE WITH USE. THIS OCCURRED DURING A DIAPHYSECTOMY OF PROXIMAL TIBIA PROCEDURE ON (B)(6) 2023. NO PIECE BROKE OFF INSIDE THE PATIENT. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. ADDITIONAL INFORMATION HAS BEEN REQUESTED.
Patient problems: Full thickness (Third Degree) Burn
MAUDE report 17514582 ↗

Device details

UDI-DI	`00888867263703`
Brand	Arthrex®
Model	AR-8750-05
Company	Arthrex, Inc.
Product code	HTW · BIT, DRILL
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Nov 28, 2022

Device type (GMDN): Cannulated surgical drill bit, single-use

A metal shaft intended to be mounted into an appropriate surgical power tool (e.g., a pneumatic reamer or drilling system handpiece with appropriate torque capacity) and rotated to bore into hard/tough tissues (e.g., bone, cartilage) in order to clear a channel of the same diameter as the shaft, typically for the insertion of a prosthetic device or other orthopaedic implant. It has a hollow centre so it can be fed over a drill guiding pin, and may be flexible; devices to assist the procedure (e.g., drill guiding pin, manual driver) may be included. This is a single-use device.

Other BIT, DRILL devices

QUICKSET 2274-25-500
Depuy Orthopaedics, Inc. · BIT, DRILL
1,985 reports
QUICKSET 2274-35-500
Depuy Orthopaedics, Inc. · BIT, DRILL
770 reports
QUICKSET 2274-30-500
Depuy Orthopaedics, Inc. · BIT, DRILL
761 reports
NA 03.037.022
Synthes GmbH · BIT, DRILL
339 reports
NA 323.062
Synthes GmbH · BIT, DRILL
309 reports
QUICKSET 2274-56-000
Depuy (Ireland) · BIT, DRILL
275 reports
QUICKSET 2274-45-500
Depuy Orthopaedics, Inc. · BIT, DRILL
211 reports
LCS 2366-83-000
Depuy (Ireland) · BIT, DRILL
207 reports

All BIT, DRILL devices →

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.

How reports and recalls are matched · Editorial policy · Report an error on this page