A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEMLOW PLATE LEFTRecalls & reported problems across all models
Biomet Orthopedics, LLC · 2 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls
- 1
We found 2 models of A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEMLOW PLATE LEFT by Biomet Orthopedics, LLC in the FDA's device registry (GUDID). Together they are named in 1 adverse event report in the FDA's MAUDE database, received between Mar 18, 2025 and Mar 18, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Fracture” (1 report).
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
A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEMLOW PLATE LEFT 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.
- May 14, 2020Class IITerminated
Distributed to the field without having completed design history files or design transfer activities
Z-2316-2020 · Root cause: Device Design · Recall details · FDA record ↗
Most reported A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEMLOW PLATE LEFT problems
Device problems
- Fracture1
Patient problems
- Failure of Implant1
A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEMLOW PLATE LEFT models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- A.L.P.S.® PROXIMAL HUMERUS PLATING SYSTEMLOW PLATE LEFT 110030109Plate, fixation, bone1 recall0 reports
- A.L.P.S.® PROXIMAL HUMERUS PLATING SYSTEMLOW PLATE LEFT 110030103Plate, fixation, bone1 report
Recent A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEMLOW PLATE LEFT adverse event reports
The 1 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryMar 18, 2025Fracture; Fracture
IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION SURGERY APPROXIMATELY SIX (6) MONTHS POST-IMPLANTATION DUE TO FRACTURING OF THE PLATE. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Failure of Implant
MAUDE report 21630919 ↗
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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