Integra® 3711062Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Frontal Sinus Recess Giraffe Forceps, 90 °, 2 mm Horizontal Jaws · Class 1
- 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 10381780076094), received between Oct 12, 2022 and Oct 12, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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.
Most reported problems
Device problems
- Break1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 12, 2022Break; Break
IT WAS REPORTED THAT THE WORKING ELEMENT OF THE GIRAFFE 90 DEGREE HORIZONTAL FORCEPS (3711062) BROKE OFF IN THE PATIENT'S NASAL CAVITY DURING SINUS SURGERY AND COULD NOT BE RETRIEVED. IT IS UNKNOWN IF A SURGICAL DELAY OCCURRED. ADDITIONAL INFORMATION HAS BEEN REQUESTED.
Patient problems: Foreign Body In Patient
MAUDE report 15589553 ↗
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
- Integra® 3711063Integra Lifesciences Production Corporation · FORCEPS, ENT2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.