DVR CROSSLOCKRecalls & reported problems across all models
Biomet Orthopedics, LLC · 5 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 5 models of DVR CROSSLOCK 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 Jan 14, 2021 and Jun 28, 2022 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Packaging Problem” (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
DVR CROSSLOCK 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.
- Feb 14, 2022Terminated
Packaging of various implants may not have sufficient adhesion on all sides, leading to loss of sterile barrier integrity. Use of product poses risk of infection, leading to surgical intervention, and/or extension of surgery to find another part.
Z-0810-2022 · Root cause: Under Investigation by firm · names 3 of these models · Recall details · FDA record ↗
Most reported DVR CROSSLOCK problems
Device problems
- Packaging Problem1
- Unsealed Device Packaging1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Patient Involvement1
DVR CROSSLOCK models
5 models, most reported first. Each model has its own page with its reports, recalls and device details.
- DVR® CROSSLOCK 1318-12-126Plate, fixation, bone1 recall0 reports
- DVR® CROSSLOCK 1318-12-176Plate, fixation, bone1 recall0 reports
- DVR® CROSSLOCK 1318-22-126Plate, fixation, bone1 recall0 reports
- DVR® CROSSLOCK 1318-21-041APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE1 report
- DVR® CROSSLOCK 1318-22-051APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE1 report
Recent DVR CROSSLOCK adverse event reports
The 2 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionJun 28, 2022Unsealed Device Packaging; Unsealed Device Packaging
IT WAS REPORTED THAT DURING PRODUCT INSPECTION IN THE WAREHOUSE, THE PRODUCT IS OUT OF THE PROTECTIVE COVER. NO PATIENT WAS INVOLVED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14843468 ↗MalfunctionJan 14, 2021Packaging Problem; Packaging Problem
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Patient Involvement
MAUDE report 11172820 ↗
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 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