Class IIOngoingZ-1295-2025
Integra LifeSciences Corp. recalls AURORA Surgiscope System
Possibility for the obturator to break (separate).
- Neurological Endoscope
- Process control
Integra LifeSciences C…NJMar 12, 2025
Integra LifeSciences Corp. recalls
The FDA has posted 5 enforcement recalls from Integra LifeSciences Corp. since 2025, none of them Class I (most serious). Most recent report: Mar 12, 2025.
Class II: 5
Latest recalls
View all 5 in the recall browser →Class IIOngoingZ-1168-2025
Integra LifeSciences Corp. recalls Brand Name: MediHoney¿ Gel Product Name: MediHoney¿ Wound & Burn Dressing Gel Model/C…
Potential that the induction seal is not completely sealed to the device tube packaging.
- Drug Wound Dressing
- Process control
Integra LifeSciences C…NJFeb 19, 2025
Class IIOngoingZ-0977-2025
Integra LifeSciences Corp. recalls CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Number: 828810…
Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.
- Central Nervous System And Components Shunt
- Labeling Change Control
Integra LifeSciences C…NJJan 29, 2025
Class IIOngoingZ-0979-2025
Integra LifeSciences Corp. recalls CODMAN CERTAS Plus Programmable Valve Right Angle Valve Only. Model Number: 828820.…
Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.
- Central Nervous System And Components Shunt
- Labeling Change Control
Integra LifeSciences C…NJJan 29, 2025
Class IIOngoingZ-0978-2025
Integra LifeSciences Corp. recalls CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Number: 828810PL.…
Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.
- Central Nervous System And Components Shunt
- Labeling Change Control
Integra LifeSciences C…NJJan 29, 2025
Firm name as filed with the FDA: “Integra LifeSciences Corp.”. Related firm entities may file under separate names. Source: U.S. FDA openFDA device enforcement reports. Informational only — verify with the FDA before acting.