Recall Register

Integra LifeSciences Corp. (NeuroSciences): FDA recalls

FDA enforcement reports name Integra LifeSciences Corp. (NeuroSciences) as the recalling firm in 13 events. The events have 31 product records. The recalls started from 2025 to 2026. All the events are device recalls.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Enforcement events

13 events, newest first.

FDA enforcement events of Integra LifeSciences Corp. (NeuroSciences)
InitiatedProduct (first record)TypeClassRecordsStatus
5 Jun 2026OmniTract Surgical Retractor System, which includes 633 of the firm s product codes.DeviceClass II1Ongoing
10 Apr 2026Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. The CerebroFlo EVD Catheter is a 3.3 mm diameter (10 Fr.), 35 cm long polyurethane catheter for diverting cerebrospinal fluid (CSF) from the ventricles of the brain through a series of drainage holes near the catheter's…DeviceClass II1Ongoing
19 Mar 2026Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.DeviceClass II5Ongoing
6 Mar 2026CUSA Clarity C7000 Console, Software Version: 2.1.1.909. Ultrasonic surgical aspirator system.DeviceClass II1Ongoing
16 Jan 2026MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: (1) 31805, (2) 31815. MediHoney Gel dressing with Active Leptospermum Honey provides a moist environment conducive to wound healing and is indicated for light to moderately exuding wounds.DeviceClass II3Ongoing
12 Dec 2025Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR Basic Kit is indicated when direct ICP monitoring is required. The kit is indicated for use in both subdural and intraparenchymal pressure monitoring applications only.DeviceClass II2Ongoing
3 Oct 2025TruDi Navigation System - Multi Instrument Adapter; - Manufacturer's Product Number (Catalog Number): EM-2025-000F Rev 00 or Rev 01;DeviceClass II1Ongoing
26 Sep 2025CODMAN Disposable Perforator 11mm. Cranial Perforator.DeviceClass I2Ongoing
5 Aug 2025Brand Name: MediHoney Product Name: MediHoney Paste Model/Catalog Number: 31505 Product Description: MediHoney Paste with Active Leptospermum Honey is a moist dressing made of 100% Active Leptospermum medical grade Honey. The dressing helps maintain a moist environment conducive to wound healing and helps aid and…DeviceClass II8Ongoing
23 May 2025MicroMyst Applicator, Box of 5. Consisting of a multilumen applicator and filtered line for use with the Integra Flow Source for the controlled application of two liquids.DeviceClass I1Ongoing
22 May 2025Extended Tip Applicator, 8CM, Box of 5.DeviceClass I3Ongoing
11 Apr 2025CODMAN Disposable Perforator, 14mm. Cranial perforator.DeviceClass I2Ongoing
4 Apr 2025INSPIRA AIR BALLOON DILATION SYSTEM 10x40, 1 PK. Airway balloon dilation catheter.DeviceClass II1Ongoing

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Recalling firm: The firm that the FDA record names for a recall.

Type and class

Integra LifeSciences Corp. (NeuroSciences): events for each product type
TypeEvents
Device13
Integra LifeSciences Corp. (NeuroSciences): events in each class
ClassEvents
Class II9
Class I4
Share of the events of the firm in Class I
31%
Share of all events on the register in Class I
18%
Events with the status Ongoing
13

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Events by year

FDA enforcement events of Integra LifeSciences Corp. (NeuroSciences), by the year that the recall started. The largest year is 2025, with 8 events.

Official channels

Cite this page

Recall Register. Integra LifeSciences Corp. (NeuroSciences): FDA recalls. https://recallregister.com/firm/integra-lifesciences-corp-neurosciences/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
State of the firm address
NJ

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not compare one firm with a different firm. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of Integra LifeSciences Corp. (NeuroSciences) have?
Class II: 9 events. Class I: 4 events. The class is for the product of a recall. It is not a class of the firm.
What is the newest FDA recall of Integra LifeSciences Corp. (NeuroSciences)?
FDA event 99193, which the firm started on 5 Jun 2026. The first product in the record is: OmniTract Surgical Retractor System, which includes 633 of the firm s product codes.
How many FDA recalls of Integra LifeSciences Corp. (NeuroSciences) have the status Ongoing?
13 events have the status Ongoing in the openFDA file. openFDA says about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.