Integra LifeSciences Corp.
217 recalls on record · Latest: Mar 12, 2025
Integra LifeSciences Corp. Recall Insight
Integra LifeSciences Corp. appears on 217 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.213% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Mar 12, 2025, which is the anchor point for assessing whether enforcement is currently active or historical.
On this page of 50 entries, severity tagging shows 1 critical, 48 moderate, and 1 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Dec 18, 2019 to Dec 13, 2023.
Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.
Integra Cranial Access Kit-For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: HITHSP04
Integra¿ Cranial Access Kit-For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: HITHSP06
Integra Cranial Access Kit -For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: INS7270
Integra Cranial Access Kit-For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: INS7260
Integra Cranial Access Kit- For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: INS7250
Integra¿ Cranial Access Kit-For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: INS7280
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
Codman Cranial Hand Drill- Indicated when a craniotomy is required for placement of an intracranial pressure (ICP) monitoring device and/or cerebrosp…
Codman Surgical Patties, Part number 801400; SURG PATXRAY 1/2X1/2-200; Lot 6396457
CereLink ICP Monitor; Catalog No. 826820, 826820P. Intracranial pressure monitor.
Integra Universal Flexible Arm part number REF 1362275
Codman Cranial Access Kits- indicated when a craniotomy is required for placement of an intracranial pressure (ICP) monitoring device and/or cerebros…
Codman Cranial Access Kits- indicated when a craniotomy is required for placement of an intracranial pressure (ICP) monitoring device and/or cerebros…
CODMAN RANEY SCALP CLIPS-Disposable cylindrical clips designed to provide hemostasis to the scalp wound edge. Part Number: 201037
CODMAN HAKIM BACTISEAL Shunt System Clear with Barium Stripe Peritoneal Catheter 120cm, with drainage Holes and Marking. For use in the treatment of …
Bactiseal Ventricular Catheter with Bactiseal Shunt System - Product Usage: use in the treatment of hydrocephalus as a component of a shunt system wh…
Bactiseal Endoscopic Ventricular Catheter: EVC- Catheter is designed for use in the treatment of hydrocephalus when shunting cerebrospinal fluid (CS…
Instruction Manual for Mayfield A2000 Skull Cap - Product Usage: intended for or rigid skeletal fixation during neurosurgical procedures. P/N: 451A20…
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. T…
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 cut…
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 tre…
NeuraGen Nerve Guide, 7mm diameter, 2cm length; Part number PNG72 - Product Usage: NeuraGen nerve guide is indicated for the repair of peripheral ner…
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
Nearby Manufacturers
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Data Sources
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.