VariAx 57-10304Recalls & reported problems
Stryker GmbH · 1.7 S VARIAX HAND LOCK PLATE, STRAIGHT · Class 2 · Implant
All models of VARIAX (345)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613154496280), received between Dec 6, 2023 and Dec 6, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (1 report).
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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
- Fracture1
Patient problems
- Failure of Implant1
- Nonunion/Delayed-union Bone Fracture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 6, 2023Break; Fracture; Break; Fracture
IT WAS REPORTED THAT THE PATIENT HAD A CRUSH OF HAND INJURY THAT WAS TREATED BY ORIF WITH A 4 HOLE PLATE ON (B)(6) 2023. THE PLATE BROKE IN SITU AND WAS IDENTIFIED BY X-RAYS. THE PLATE WAS REMOVED ON (B)(6) 2023.
Patient problems: Failure of Implant; Nonunion/Delayed-union Bone Fracture
MAUDE report 18275729 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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