Integra LifeSciences Corp.
217 recalls on record · Latest: Mar 12, 2025
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Agency notice ledger
Federal filing book Integra LifeSciences Corp. HEAVY-BOOK · SINGLE-AGENCY
#63 of 14,151 · 217 notices · 0.208% archive
- BOOK 217 notices
- RANK #63 of 14,151
- SHARE 0.208% archive
- AGENCY FDA Devices (217)
- CAT medical devices
- CATS 1 category
- LATEST Mar 12, 2025
- PHOTO Sunland, Incorporated
Nearest notice-volume peer: Sunland, Incorporated (2 notice gap)
Integra LifeSciences Corp. accounts for about 0.208% of the 104,423-notice archive on 217 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →
How Integra LifeSciences Corp. compares to 14,151 recalling firms
Integra LifeSciences Corp. ranks 63rd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.
Integra LifeSciences Corp. vs all firms by recall-notice count
Where this firm's archive sits among every tracked recalling manufacturer
217 63rd of 14151 higher than 14,088 of 14,151 firms
Firms, banded by distinct federal recall-event inventory
Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13
Integra LifeSciences Corp. in the notice-volume neighbourhood
Distinct federal recall events among this firm and nearest nationwide peers
- Biomet 3i, LLC
Biomet 3i, LLC
222 notices
- Ortho-Clinica…
Ortho-Clinical Diagnostics
221 notices
- Sunland, Inco…
Sunland, Incorporated
219 notices
- Integra LifeS… (this)
Integra LifeSciences Corp.
217 notices
- Exactech, Inc.
Exactech, Inc.
211 notices
- Medtronic Vas…
Medtronic Vascular
211 notices
What this shows Integra LifeSciences Corp. holds about 0.208% of archive notices alongside 217 distinct filings.
FDA Devices Moderate Dec 13, 2023
Integra Cranial Access Kit-For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: HITHSP04
FDA Devices Moderate Dec 13, 2023
Integra¿ Cranial Access Kit-For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: HITHSP06
FDA Devices Moderate Dec 13, 2023
Integra Cranial Access Kit -For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: INS7270
FDA Devices Moderate Dec 13, 2023
Integra Cranial Access Kit-For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: INS7260
FDA Devices Moderate Dec 13, 2023
Integra Cranial Access Kit- For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: INS7250
FDA Devices Moderate Dec 13, 2023
Integra¿ Cranial Access Kit-For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: INS7280
FDA Devices Moderate Dec 13, 2023
Combo Kit Consists OF 10-110/INS-4500/INS-7040- For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: 31004
FDA Devices Moderate May 31, 2023
Codman Cranial Hand Drill- Indicated when a craniotomy is required for placement of an intracranial pressure (ICP) monitoring device and/or cerebrospinal fluid drainage device. Part Number: 82-6607
FDA Devices Moderate Jan 18, 2023
Codman Surgical Patties, Part number 801400; SURG PATXRAY 1/2X1/2-200; Lot 6396457
FDA Devices Critical Aug 3, 2022
CereLink ICP Monitor; Catalog No. 826820, 826820P. Intracranial pressure monitor.
FDA Devices Moderate Apr 20, 2022
Integra Universal Flexible Arm part number REF 1362275
FDA Devices Moderate Mar 30, 2022
Codman Cranial Access Kits- indicated when a craniotomy is required for placement of an intracranial pressure (ICP) monitoring device and/or cerebrospinal fluid drainage procedures. Part Number: 826616
FDA Devices Moderate Mar 30, 2022
Codman Cranial Access Kits- indicated when a craniotomy is required for placement of an intracranial pressure (ICP) monitoring device and/or cerebrospinal fluid drainage procedures. Product umber: 826614
FDA Devices Moderate Aug 18, 2021
CODMAN RANEY SCALP CLIPS-Disposable cylindrical clips designed to provide hemostasis to the scalp wound edge. Part Number: 201037
FDA Devices Moderate Apr 14, 2021
CODMAN HAKIM BACTISEAL Shunt System Clear with Barium Stripe Peritoneal Catheter 120cm, with drainage Holes and Marking. For use in the treatment of hydrocephalus. Catalog Number: NS5524
FDA Devices Moderate Dec 30, 2020
Bactiseal Ventricular Catheter with Bactiseal Shunt System - Product Usage: use in the treatment of hydrocephalus as a component of a shunt system when draining or shunting cerebrospinal fluid (CSF) Part Number: 823073
FDA Devices Moderate Dec 30, 2020
Bactiseal Endoscopic Ventricular Catheter: EVC- Catheter is designed for use in the treatment of hydrocephalus when shunting cerebrospinal fluid (CSF) from the ventricles of the brain. Part Number: 823087
FDA Devices Moderate Dec 16, 2020
Instruction Manual for Mayfield A2000 Skull Cap - Product Usage: intended for or rigid skeletal fixation during neurosurgical procedures. P/N: 451A2000
FDA Devices Moderate Sep 23, 2020
Integra Padgett Dermatome Set - Product Usage: are intended for use in the cutting of skin grafts for use in plastic surgery and/or burn treatment. These instruments are intended only for professional use in hospitals and similar medical facilities, where the patient will be under the supervision of trained personnel.
FDA Devices Moderate Sep 23, 2020
13 ft Handpiece Cable, component of the Dermatome Sets Model S and Model S6 and also as a spare part - Product Usage: are intended for use in the cutting of skin grafts for use in plastic surgery and/or burn treatment. These instruments are intended only for professional use in hospitals and similar medical facilities, where the patient will be under the supervision of trained personnel.
FDA Devices Moderate Sep 23, 2020
Integra Padgett Electric Dermatome Set - Product Usage: are intended for use in the cutting of skin grafts for use in plastic surgery and/or burn treatment. These instruments are intended only for professional use in hospitals and similar medical facilities, where the patient will be under the supervision of trained personnel.
FDA Devices Low Mar 18, 2020
NeuraGen Nerve Guide, 7mm diameter, 2cm length; Part number PNG72 - Product Usage: NeuraGen nerve guide is indicated for the repair of peripheral nerve discontinuities where gap closure can be achieved by flexion of the extremity.
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
FDA Devices Moderate Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
Integra LifeSciences Corp. carries an outsized archive share
Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.
Similar recall count
Nearest multi-notice firms by distinct-event totals (217 here — heavy-book).
Similar medical devices volume
Nearest multi-notice firms in the same narrow category lane.
Frequently Asked Questions
How many federal recall notices name Integra LifeSciences Corp.? ▼
PlainRecalls indexes 217 distinct federal recall events naming Integra LifeSciences Corp., aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Integra LifeSciences Corp. sit among other recalling firms? ▼
Integra LifeSciences Corp. ranks #63 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Integra LifeSciences Corp.'s notices? ▼
FDA Devices accounts for 217 of this firm's 217 indexed notices.
What product category dominates Integra LifeSciences Corp.'s filing book? ▼
Filings for Integra LifeSciences Corp. span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Integra LifeSciences Corp.: 217 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.
Firm-level totals aggregate distinct federal recall events naming Integra LifeSciences Corp.; individual notices remain authoritative on each linked recall page.
Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026