LATERA LATANI20Recalls & reported problems
Stryker Corporation · Absorbable Nasal Implants 20mm · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00857037006013), received between Jan 30, 2025 and Jan 30, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Patient Device Interaction Problem1
Patient problems
- Failure of Implant1
- Obstruction/Occlusion1
- Pain1
- Swelling/ Edema1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 30, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
IT WAS REPORTED VIA MEDWATCH THAT A PATIENT'S NASAL IMPLANTS HAVE NOT ABSORBED AFTER 18 MONTHS OF IMPLANTATION. THE PATIENT REPORTED CHRONIC PAIN, SWELLING, AND DIFFICULTY BREATHING AS A RESULT OF OBSTRUCTED NASAL VALVES. ADDITIONAL INFORMATION IS CURRENTLY BEING REQUESTED.
Patient problems: Failure of Implant; Obstruction/Occlusion; Pain; Swelling/ Edema
MAUDE report 21274596 ↗
Other Polymer, Ear, Nose And Throat, Synthetic, Absorbable devices
- Otopore 5400020100Stryker Corporation · POLYMER, EAR, NOSE AND THROAT, SYNTHETIC, ABSORBABLE1 recall0 reports
- Otopore 5400010000Stryker Corporation · POLYMER, EAR, NOSE AND THROAT, SYNTHETIC, ABSORBABLE1 recall0 reports
- PuraSinus 5mL 651-0093-D Matrix Inc. · Polymer, Ear, Nose And Throat, Synthetic, Absorbable1 recall0 reports
- Otopore 5400020000Stryker Corporation · POLYMER, EAR, NOSE AND THROAT, SYNTHETIC, ABSORBABLE1 recall0 reports
- LATERA LATANI02Stryker Corporation · Polymer, Ear, Nose And Throat, Synthetic, Absorbable12 reports
- LATERA LATSYS24Stryker Corporation · Polymer, Ear, Nose And Throat, Synthetic, Absorbable8 reports
- LATERA LATSYS20Stryker Corporation · Polymer, Ear, Nose And Throat, Synthetic, Absorbable3 reports
- 1.5 LACTOSORB SYSTEM 915-2315Biomet Microfixation, Inc · POLYMER, EAR, NOSE AND THROAT, SYNTHETIC, ABSORBABLE3 reports
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 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