LATERA LATSYS20Recalls & reported problems
Stryker Corporation · Absorbable Nasal Implant System 20mm · Class 2 · Implant
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00857037006037), received between Oct 15, 2025 and Jul 22, 2026 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Migration” (2 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, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Migration2
- Patient Device Interaction Problem1
Patient problems
- Unspecified Tissue Injury2
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Subcutaneous Nodule1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 22, 2026Migration
Patient problems: Unspecified Tissue Injury
MAUDE report 25907863 ↗MalfunctionJul 22, 2026Patient Device Interaction Problem
Patient problems: Subcutaneous Nodule
MAUDE report 25907796 ↗InjuryOct 15, 2025Migration; Migration
THE PATIENT WAS REIMPLANTED ON THE RIGHT NASAL ANATOMY AND NO FURTHER ISSUES HAVE BEEN NOTED.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Unspecified Tissue Injury
MAUDE report 23301418 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.