NA 6020-13-000Recalls & reported problems

Depuy (Ireland) · PLAIN HOOK W/DISK 17in · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports: 2
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295178392), received between Dec 14, 2022 and Aug 14, 2023 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (2 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.

Most reported problems

Device problems

Break2

Patient problems

No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

MalfunctionAug 14, 2023Break; Break
DURING STERILIZATION, THE CURETTE WAS FOUND TO BE BROKEN AND UNUSABLE. NO PATIENT CONSEQUENCE OR SURGICAL DELAY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17542876 ↗
MalfunctionDec 14, 2022Break; Break
IT WAS REPORTED THAT THERE WERE 2 HOOKS THAT HAVE BROKEN TIPS. THIS DID NOT DELAY A SURGERY, IT WAS NOTICED BEFORE USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15979163 ↗

Device details

UDI-DI	`10603295178392`
Brand	NA
Model	6020-13-000
Catalog no.	602013000
Company	Depuy (Ireland)
Product code	KIK · HOOK, BONE
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	—
Single use	No
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	May 28, 2026

Device type (GMDN): Bone hook

A hand-held, surgical instrument used for hooking around or into bone, typically to grasp, hold, and apply traction to the bone during a surgical intervention. It is a shaft-like instrument with a robust design and can have a singular hook or multiple hooks at the distal end and a handle of various designs at the proximal end. It is made of high-grade stainless steel. It is sometimes called a bone retractor. This is a reusable device.

Other HOOK, BONE devices

MORELAND 2422-03-000
Depuy Orthopaedics, Inc. · HOOK, BONE
3 reports
V. Mueller OS4080-002
Steris Corporation · HOOK, BONE
1 report

All HOOK, BONE 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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