RESORB XG, STERILE 52-808-13-04Recalls & reported problems
KLS-Martin L.P. · MESH, SMALL GRID, PLLA-PGA · Class 2 · Implant
Data updated Oct 18, 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 00888118001450), received between Jun 14, 2022 and Jun 14, 2022 — classified as 1 injury.
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 18, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Impaired Healing1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 14, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT A PORTION OF A PLATE WAS REMOVED. DUE TO IT BEING EXPOSED.
Patient problems: Impaired Healing
MAUDE report 14690971 ↗
Other FASTENER, PLATE, CRANIOPLASTY devices
- RapidSorb 530.553.01SSynthes GmbH · FASTENER, PLATE, CRANIOPLASTY1 recall0 reports
- "1.5MM" SYSTEM 95-6104Biomet Microfixation, Inc · FASTENER, PLATE, CRANIOPLASTY30 reports
- "1.5MM" SYSTEM 95-6105Biomet Microfixation, Inc · FASTENER, PLATE, CRANIOPLASTY16 reports
- UNIVERSAL NEURO 3 56-15904Stryker Leibinger GmbH & Co. KG · FASTENER, PLATE, CRANIOPLASTY7 reports
- 1.5MM SYSTEM 91-6104-50Biomet Microfixation, Inc · FASTENER, PLATE, CRANIOPLASTY6 reports
- 1.5MM SYSTEM 91-6105XBiomet Microfixation, Inc · FASTENER, PLATE, CRANIOPLASTY5 reports
- Universal Neuro 3 56-15934Stryker Leibinger GmbH & Co. KG · FASTENER, PLATE, CRANIOPLASTY4 reports
- Universal Neuro 3 56-15034Stryker Leibinger GmbH & Co. KG · FASTENER, PLATE, CRANIOPLASTY2 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 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 18, 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