Integra® Miltex® V916-160Recalls & reported problems

Integra Lifesciences Production Corporation · Integra® Miltex® Doyen Intestinal Forceps, 9" Straight · Class 1

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 10381780414506), received between Feb 13, 2025 and Feb 13, 2025 — classified as 1 injury.

The most frequently reported specific device problem is “Material Fragmentation” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Reports received per month

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Material Fragmentation1

Patient problems

No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

InjuryFeb 13, 2025Material Fragmentation; Material Fragmentation
N/A
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21374400 ↗

Device details

UDI-DI	`10381780414506`
Brand	Integra® Miltex®
Model	V916-160
Company	Integra Lifesciences Production Corporation
Product code	HRQ · HEMOSTAT
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	No
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Apr 27, 2023

Device type (GMDN): Surgical soft-tissue manipulation forceps, scissors-like, reusable

A hand-held, manual, open-surgery instrument designed to grasp, manipulate, dissect, and/or clamp soft-tissues (e.g., organs, blood vessels); it is not intended for grasping/clamping bone or teeth, nor is it dedicated to ophthalmic surgery and is not a dedicated biopsy device. It has a scissors-like hinged design with ring handles and blades (non-cutting) that may be available in a range of sizes or designs. It may be intended for use at a specific anatomy. This is a reusable device intended to be sterilized prior to use.

Other HEMOSTAT devices

Centurion 66695
Centurion Medical Products Corporation · HEMOSTAT
2 recalls0 reports
AESCULAP BH145R
Aesculap AG · HEMOSTAT
1 recall5 reports
AESCULAP BH443R
Aesculap AG · HEMOSTAT
1 recall2 reports
AESCULAP BH135R
Aesculap AG · HEMOSTAT
1 recall1 report
AESCULAP BH207R
Aesculap AG · HEMOSTAT
1 recall0 reports
AESCULAP BH334R
Aesculap AG · HEMOSTAT
1 recall0 reports
AESCULAP BH645R
Aesculap AG · HEMOSTAT
1 recall0 reports
AESCULAP BH653R
Aesculap AG · HEMOSTAT
1 recall0 reports

All HEMOSTAT devices →

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