PEG FULLY THREADED, LOCKINGRecalls & reported problems across all models
Biomet Orthopedics, LLC · 3 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls
- 1
We found 3 models of PEG FULLY THREADED, LOCKING by Biomet Orthopedics, LLC in the FDA's device registry (GUDID). Together they are named in 2 adverse event reports in the FDA's MAUDE database, received between Dec 16, 2025 and Dec 16, 2025 — classified as 2 injuries.
The most frequently reported specific device problem is “Difficult to Remove” (2 reports).
1 FDA recall record name at least one of these models by its device identifier.
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
PEG FULLY THREADED, LOCKING recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Jul 12, 2018Class IITerminated
A size 22mm threaded peg was found in the package of a 10mm unit.
Z-2965-2018 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported PEG FULLY THREADED, LOCKING problems
Device problems
- Difficult to Remove2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
PEG FULLY THREADED, LOCKING models
3 models, most reported first. Each model has its own page with its reports, recalls and device details.
- PEG FULLY THREADED, LOCKING 1312-12-610PLATE, FIXATION, BONE1 recall0 reports
- PEG FULLY THREADED, LOCKING 1312-12-618PIN, FIXATION, THREADED1 report
- PEG FULLY THREADED, LOCKING 1312-12-622ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES1 report
Recent PEG FULLY THREADED, LOCKING adverse event reports
The 2 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryDec 16, 2025Difficult to Remove; Difficult to Remove
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23817458 ↗InjuryDec 16, 2025Difficult to Remove; Difficult to Remove
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23817432 ↗
Other Biomet Orthopedics, LLC products
- AFFIXUSHIP FRACTURE NAIL - RIGHT39 models · 6 reports · 37 recalls
- AFFIXUSHIP FRACTURE NAIL - LEFT27 models · 7 reports · 24 recalls
- Compress Device71 models · 99 reports · 22 recalls
- Arcos Modular Revision Hip System71 models · 191 reports · 19 recalls
- Comprehensive Reverse Shoulder57 models · 895 reports · 3 recalls
- Vanguard Knee System147 models · 306 reports · 13 recalls
- STAGEONE17 models · 0 reports · 18 recalls
- StageOne Select15 models · 2 reports · 15 recalls
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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