Integra LifeSciences Corp.
150 recalls on record · Latest: Mar 12, 2025
Integra LifeSciences Corp. Recall Insight
Integra LifeSciences Corp. appears on 150 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.179% 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 3 critical, 47 moderate, and 0 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 Apr 24, 2019 to Dec 18, 2019.
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.
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
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
Cerelink ICP Monitor, Model Number 826820; intended for use as an interface between compatible strain-gauge type pressure transducers and standard p…
Integra Jarit GEMINI CLAMP 9 1/4 inch - used in vascular and cardiothoracic procedures used for clamping and occluding vessels. Cat. #140-332
Codman ISOCOOL Bipolar Forceps-are indicated for cauterizing, coagulating, grasping, and manipulating tissue during general surgery, neurosurgery, EN…
MoniTorr INS1100 INS-1100 CSF Drainage System used with Pole Mount System Product Usage: The MoniTorr ICP External CSF Drainage and Monitoring Sy…
LimiTorr INS9020 INS-9020 LIMITORR VOLUME LIMITING EVD 20 ML LimiTorr INS9020SP1 INS-9020SP1 LIMITORR VOLUME EVD 20ML LimiTorr INS9030 INS-9030 LIM…
MoniTorr 10100 10-100 CSF Drainage System w/Patient Line One Way Valve MoniTorr 10102 10-102 CSF Drainage System w/Patient Line One Way Valve w Mon…
Talar Dome Total Ankle Prosthesis, Flat Cut, Size 3, Right, Product No. LJU813T
Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 0, Left, Part No. LJU210T
Talar Dome Total Ankle Prosthesis , Sloped, Size 1, Left, Product No. LJV191T
Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 3, Left, Part No. LJU213T
Talar Dome Total Ankle Prosthesis , Sloped, Size 0, Left, Product No. LJV190T
Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 2, Right, Part No. LJU202T
Talar Dome Total Ankle Prosthesis, Sloped, Size 2, Left, Product No. LJV192T
Tibial Total Ankle Prosthesis Tray, Size 2, Product No. LJU222T
Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 1, Left, Part No. LJU211T
Talar Dome Total Ankle Prosthesis, Flat Cut, Size 1, Left, Product No. LJU821T
Talar Dome Total Ankle Prosthesis, Sloped, Size 2, Right, Product No. LJV182T
Talar Dome Total Ankle Prosthesis , Sloped, Size 3, Right, Product No. LJV183T
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