Captura Pro G56996Recalls & reported problems

Cook Incorporated · Forceps Without Spike · Class 2

All models of Captura Pro (15)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports: 1
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00827002569966), received between Jul 10, 2026 and Jul 10, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Failure to Cut” (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

Failure to Cut1

Patient problems

Laceration(s)1

Recent adverse event reports

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

MalfunctionJul 10, 2026Failure to Cut
Patient problems: Laceration(s)
MAUDE report 25781537 ↗

Device details

UDI-DI	`00827002569966`
Brand	Captura Pro
Model	G56996
Catalog no.	BF-2.8SJ-230-20
Company	Cook Incorporated
Product code	PTS · Endoscopic grasping/cutting instrument, non-powered, exempt
Class	Class 2
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Sep 7, 2018

Device type (GMDN): Flexible endoscopic biopsy forceps, single-use

A flexible, manual, non-electrosurgical instrument intended to obtain tissue specimens during endoscopic procedures (e.g., gastro-urological endoscopy, laparoscopy, bronchoscopy, laryngoscopy) for histopathological examination. It is typically a flexible metal coil with a pair of scissors-like cups with cutting edge rims, which are operated by a control handle at the proximal end of the instrument. It is introduced into the body through an artificial orifice of the body or the working channel of the endoscope. This is a single-use device.

Other Endoscopic grasping/cutting instrument, non-powered, exempt devices

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45 reports
Single Use Grasping Forceps FG-253SX
Olympus Medical Systems Corp. · Endoscopic grasping/cutting instrument, non-powered, exempt
27 reports
Raptor 00711177
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Captura G31576
Cook Incorporated · Endoscopic grasping/cutting instrument, non-powered, exempt
19 reports
Captura G56059
Cook Incorporated · Endoscopic grasping/cutting instrument, non-powered, exempt
18 reports
Captura G31577
Cook Incorporated · Endoscopic grasping/cutting instrument, non-powered, exempt
17 reports
Captura Pro G50697
Cook Incorporated · Endoscopic grasping/cutting instrument, non-powered, exempt
17 reports

All Endoscopic grasping/cutting instrument, non-powered, exempt 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.

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