Integra® 3711063Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Frontal Sinus Recess Giraffe Forceps, 90 °, 2 mm Vertical Jaws · Class 1
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10381780076100), received between Apr 28, 2022 and Apr 28, 2022 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Device Reprocessing Problem” (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.
Most reported problems
Device problems
- Device Reprocessing Problem2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 28, 2022Device Reprocessing Problem; Device Reprocessing Problem
THIS IS 2 OF 2 REPORTS LINKED TO MFG REPORT NUMBER 3003249645-2022-00016: IT HAS BEEN REPORTED THAT THE FORCEPS 3711063 GIRAFFE WAS NOT SUITABLE TO ENSURE COMPLETE STERILIZATION. THE FACILITY HAS NOT REPORTED IF THERE WAS PATIENT INVOLVEMENT, INJURY OR SURGICAL DELAY RELATED TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14240394 ↗MalfunctionApr 28, 2022Device Reprocessing Problem; Device Reprocessing Problem
THIS IS 1 OF 2 REPORTS LINKED TO MFG REPORT NUMBER 3003249645-2022-00017: IT HAS BEEN REPORTED THAT THE FORCEPS 3711063 GIRAFFE WAS NOT SUITABLE TO ENSURE COMPLETE STERILIZATION. THE FACILITY HAS NOT REPORTED IF THERE WAS PATIENT INVOLVEMENT, INJURY OR SURGICAL DELAY RELATED TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14240318 ↗
Other FORCEPS, ENT devices
- AESCULAP BH952RAesculap AG · FORCEPS, ENT1 recall0 reports
- AESCULAP BH959RAesculap AG · FORCEPS, ENT1 recall0 reports
- AESCULAP BH965RAesculap AG · FORCEPS, ENT1 recall0 reports
- AESCULAP BH957RAesculap AG · FORCEPS, ENT1 recall0 reports
- AESCULAP BH961RAesculap AG · FORCEPS, ENT1 recall0 reports
- AESCULAP BH951RAesculap AG · FORCEPS, ENT1 recall0 reports
- AESCULAP BH963RAesculap AG · FORCEPS, ENT1 recall0 reports
- V. Mueller RH551-111Steris Corporation · FORCEPS, ENT2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.