Integra LifeSciences Corp. (NeuroSciences)

Frequent Recalls

7

Recalls

0

Units Recalled

0

Injuries

0

Deaths

Categories: Medical Device

2026-04-22 to 2026-05-20

Date	Source	Product	Brand	Severity	Units
2026-05-20	FDA Device	FDA Recall: Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. T	Integra LifeSciences Corp. (NeuroSciences)	Class II	N/A
2026-04-29	FDA Device	FDA Recall: CUSA Clarity C7000 Console, Software Version: 2.1.1.909. Ultrasonic surgical aspirator system.	Integra LifeSciences Corp. (NeuroSciences)	Class II	N/A
2026-04-22	FDA Device	FDA Recall: Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.	Integra LifeSciences Corp. (NeuroSciences)	Class II	N/A
2026-04-22	FDA Device	FDA Recall: Cytal Burn Matrix 10x15 cm. Product ID: BMM1015.	Integra LifeSciences Corp. (NeuroSciences)	Class II	N/A
2026-04-22	FDA Device	FDA Recall: Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.	Integra LifeSciences Corp. (NeuroSciences)	Class II	N/A
2026-04-22	FDA Device	FDA Recall: Cytal Burn Matrix 7x10 cm. Product ID: BMM0710.	Integra LifeSciences Corp. (NeuroSciences)	Class II	N/A
2026-04-22	FDA Device	FDA Recall: Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710.	Integra LifeSciences Corp. (NeuroSciences)	Class II	N/A