SELF CENTERINGRecalls & reported problems across all models

Depuy (Ireland) · 29 models in the FDA device registry

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports: 1,061
Deaths reported: 0
Injuries reported: 4
Recalls: 0

We found 29 models of SELF CENTERING by Depuy (Ireland) in the FDA's device registry (GUDID). Together they are named in 1,061 adverse event reports in the FDA's MAUDE database, received between Jul 19, 2017 and Sep 29, 2026 — classified as 4 injuries, 1,057 malfunctions.

The most frequently reported specific device problem is “Device-Device Incompatibility” (361 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Reports received per month, all models

Last 36 months. The most recent month may be incomplete.

Most reported SELF CENTERING problems

Device problems

Device-Device Incompatibility361
Contamination /Decontamination Problem232
Illegible Information153
Break128
Naturally Worn121
Scratched Material114
Mechanical Jam54
Material Deformation36

Patient problems

No Clinical Signs, Symptoms or Conditions752
No Consequences Or Impact To Patient217
Insufficient Information71
No Code Available15
Not Applicable13
No Information12
Foreign Body In Patient1
No Known Impact Or Consequence To Patient1

SELF CENTERING models

29 models, most reported first. Each model has its own page with its reports, recalls and device details.

SELF CENTERING 2055-13-000
IMPACTOR
324 reports
SELF CENTERING 2055-12-000
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
145 reports
SELF CENTERING 2055-16-000
TEMPLATE
132 reports
SELF CENTERING 2055-50-000
TEMPLATE
45 reports
SELF CENTERING 2055-48-000
TEMPLATE
43 reports
SELF CENTERING 2055-46-000
TEMPLATE
36 reports
SELF CENTERING 2055-45-000
TEMPLATE
35 reports
SELF CENTERING 2055-49-000
TEMPLATE
31 reports
SELF CENTERING 2055-47-000
TEMPLATE
29 reports
SELF CENTERING 2055-51-000
TEMPLATE
28 reports
SELF CENTERING 2055-52-000
TEMPLATE
24 reports
SELF CENTERING 2055-44-000
TEMPLATE
22 reports
SELF CENTERING 2055-43-000
TEMPLATE
21 reports
SELF CENTERING 2055-53-000
TEMPLATE
18 reports
SELF CENTERING 2055-54-000
TEMPLATE
18 reports
SELF CENTERING 2055-56-000
TEMPLATE
12 reports
SELF CENTERING 2055-14-000
EXTRACTOR
10 reports
SELF CENTERING 2055-40-000
TEMPLATE
10 reports
SELF CENTERING 2055-41-000
TEMPLATE
10 reports
SELF CENTERING 2055-58-000
TEMPLATE
9 reports
SELF CENTERING 2055-61-000
TEMPLATE
9 reports
SELF CENTERING 2055-39-000
TEMPLATE
8 reports
SELF CENTERING 2055-42-000
TEMPLATE
8 reports
SELF CENTERING 2055-59-000
TEMPLATE
8 reports
SELF CENTERING 2055-60-000
TEMPLATE
8 reports
SELF CENTERING 2055-57-000
TEMPLATE
7 reports
SELF CENTERING 2055-55-000
TEMPLATE
6 reports
SELF CENTERING 2055-11-000
TRAY, SURGICAL, INSTRUMENT
4 reports
SELF CENTERING 2055-65-000
TEMPLATE
1 report

Recent SELF CENTERING adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

MalfunctionSep 29, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50931386 ↗
MalfunctionSep 21, 2026Device-Device Incompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50845881 ↗
MalfunctionSep 18, 2026Device-Device Incompatibility; Mechanical Jam
It was reported that during trialing for the unipolar ball the scrub tech had difficulty applying the mod endo head trial to the handle. It eventually went on but was difficult to remove after the surgery when instruments were returned to their trays. After decontamination the reporter found one or two perimeter ball bearings did not fully depress. The reporter soaked the handle in a milk/lubricant recommended by the hospital's SPD director, which did not resolve the problem. The issue did not cause delay to the surgery. The head trial was not affected. The instrument was removed from use. All available information has been disclosed.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50820270 ↗
MalfunctionSep 10, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50721379 ↗
MalfunctionSep 10, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50721372 ↗
MalfunctionSep 10, 2026Break
It was reported that the bipolar TRL retaining clip was broken. All available information has been disclosed.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50713106 ↗
MalfunctionSep 3, 2026Device-Device Incompatibility; Mechanical Jam
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50596582 ↗
MalfunctionSep 3, 2026Illegible Information
It was reported that the size and product numbers had become unreadable. The event did not happen in surgery.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50581544 ↗
MalfunctionSep 3, 2026Illegible Information
It was reported that the size and product numbers had become unreadable. The event did not happen in surgery.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50581541 ↗
MalfunctionSep 3, 2026Illegible Information
It was reported that the size and product numbers had become unreadable. The event did not happen in surgery.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50581538 ↗
MalfunctionSep 3, 2026Illegible Information
It was reported that the size and product numbers had become unreadable. The event did not happen in surgery.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50581534 ↗
MalfunctionSep 3, 2026Illegible Information
It was reported that the size and product numbers had become unreadable. The event did not happen in surgery.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50581529 ↗
MalfunctionSep 3, 2026Illegible Information
It was reported that the size and product numbers had become unreadable. The event did not happen in surgery.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50581526 ↗
MalfunctionSep 3, 2026Illegible Information
It was reported that the size and product numbers had become unreadable. The event did not happen in surgery.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50581522 ↗
MalfunctionAug 5, 2026Break; Mechanical Jam
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50142140 ↗

Other Depuy (Ireland) products

All Depuy (Ireland) devices →

Sources and updates

Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
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.

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