GE Medical Systems Information Technologies Inc

Frequent Recalls

7

Recalls

0

Units Recalled

0

Injuries

0

Deaths

Categories: Medical Device

2026-06-03 to 2026-06-10

Date	Source	Product	Brand	Severity	Units
2026-06-10	FDA Device	FDA Recall: CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3	GE Medical Systems Information Technologies Inc	Class II	N/A
2026-06-03	FDA Device	FDA Recall: GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603-902, Produ	GE Medical Systems Information Technologies Inc	Class II	N/A
2026-06-03	FDA Device	FDA Recall: GE HealthCare ApexPro v6.0 eDelivery Software, REF #5700026, Product Code SUV; used in conjunction w	GE Medical Systems Information Technologies Inc	Class II	N/A
2026-06-03	FDA Device	FDA Recall: GE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER, REF #2108729-901, Product Code SS9; ApexP	GE Medical Systems Information Technologies Inc	Class II	N/A
2026-06-03	FDA Device	FDA Recall: GE HealthCare APEXPRO v5.0 - ARK2250 - Software Disaster Recovery USB Kit - Orderable by GE Service	GE Medical Systems Information Technologies Inc	Class II	N/A
2026-06-03	FDA Device	FDA Recall: GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL, REF #2063702-101, Product Code SS9; used in c	GE Medical Systems Information Technologies Inc	Class II	N/A
2026-06-03	FDA Device	FDA Recall: GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603, Product Code KSA;	GE Medical Systems Information Technologies Inc	Class II	N/A