Integra LifeSciences recalls

Integra LifeSciences has 246 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 12 Mar 2025. 62 are still ongoing.

Total recalls246since 2012
Last 12 months0reported
Class I52% of total
Ongoing62latest 12 Mar 2025

Recalls per month, last 24 months

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Severity split

Class I 5 2%Class II 238 97%Class III 3 1%

By year

Ongoing integra lifesciences recalls

62 active

All integra lifesciences recalls, newest first

246 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIAurora Surgiscope System, Sterile recalled by Integra LifeSciencesIntegra LifeSciencesDevice MalfunctionNationwide
DeviceCLASS IIMediHoney¿ Gel MediHoney¿ Wound & Burn Dressing Gel recalledIntegra LifeSciencesPackaging DefectsNationwide
DeviceCLASS IICodman Certas Plus Programmable Valve Inline Small Valve Only recalledIntegra LifeSciencesPackaging DefectsNationwide
DeviceCLASS IICodman Certas Plus Programmable Valve Right Angle Valve Only recalledIntegra LifeSciencesPackaging DefectsNationwide
DeviceCLASS IICodman Certas Plus Programmable Valve Inline Small Valve Only recalledIntegra LifeSciencesPackaging DefectsNationwide
DeviceCLASS IISurg Pat Xray recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IISurg Strp recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IISurg Pat Xray recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IISurg Pat Xray 1/-1/2 recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IIMicr Patie Rnd recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IIDuraform Dural Graft Implant, Size recalled by Integra LifeSciencesIntegra LifeSciencesPotency & AssayNJ
DeviceCLASS IISurg Strp recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IISurg Pat Xray recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IISurg Strp recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IISurg Pat Xray recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IISurg Strp recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IISurg Strp recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IISurg Strp recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IISurg Pat Xray 1//2 recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IISurg Strp recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IISurg Strp recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IISurg Pat Xray 1//4 recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IISurg Pat Xray 3//4 recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IISurg Pat Xray 1/-1/2 recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IISurg Pat Xray recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IISurg Pat Xray recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IISurg Strp recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IISurg Pat Xray recalled by Integra LifeSciencesIntegra LifeSciencesOtherNationwide
DeviceCLASS IIMedihoney Dressing with Active Leptospermum Honey Wound recalledIntegra LifeSciencesSterilityNationwide
DeviceCLASS IITruDi NAV Suction, 0 Degrees recalled by Integra LifeSciencesIntegra LifeSciencesOther35 states

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.