Skip to content

RapidSorb 851.724.01SRecalls & reported problems

Synthes GmbH · 1.5MM RAPID RESORB STRAIGHT ROW MESH/75X75X0.8MM THK-STER · Class 2 · Implant

All models of RapidSorb (27)

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 10887587064222), received between Jul 2, 2019 and Jul 2, 2019 — classified as 1 injury.

3 other recalls cover devices cleared under the same FDA submission (K030069, K062789); they may or may not involve this specific model.

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.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Hypersensitivity/Allergic reaction1
  • No Code Available1
  • Skin Irritation1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJul 2, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    UPDATED: IT WAS REPORTED THAT ON (B)(6) 2017, THE PATIENT UNDERWENT A SECOND SURGERY WAS PERFORMED DUE TO ALLERGIC REACTION TO THE MATERIAL UNDER THE SURGICAL SITE THAT CAUSED INFLAMMATION AND SKIN BREAKDOWN. ITEMS WERE NOT REMOVED OUT OF PATIENTS HEAD BECAUSE THEY ARE RESORBABLE AND DISSOLVE. PATIENT OPEN WOUND HAD TO BE CLEANED AND CARED FOR AND REQUIRED MORE VISITS TO THE SURGEON FOR WOUND HEALING.

    Patient problems: Hypersensitivity/Allergic reaction; No Code Available; Skin Irritation

    MAUDE report 8753298 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K030069, K062789. One submission often covers many models, so check the product and lot details in each record.

  • Z-1920-2016 · May 2, 2016 · Terminated
    1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 35 mm - Sterile, Rapid Resorbable Fixation System. 1.5 mm Rapid Resorbable Orbital Floor Plate with Bending Template. Intend
  • Z-1919-2016 · May 2, 2016 · Terminated
    1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 30 mm - Sterile, Rapid Resorbable Fixation System. 1.5 mm Rapid Resorbable Orbital Floor Plate with Bending Template. Intend
  • Z-1918-2016 · May 2, 2016 · Terminated
    1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 24 mm - Sterile, Rapid Resorbable Fixation System. 1.5 mm Rapid Resorbable Orbital Floor Plate with Bending Template. Inte

Other PLATE, BONE devices

All PLATE, BONE devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page