Recall
FDAHealthJuly 2, 2025

GE Medical Systems, LLC — GE HealthCare OEC 9900 Elite C-arm Systems.

⚠️ GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in certain OEC 9800 and OEC 9900 Elite C-arm Systems. Specifically, impacted systems are missing the full layer of lead tape in the collimator covers, which will lead to a small increase in radiation exposure to the patient and/or operator. The missing lead tape is not detectable by the user.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
July 2, 2025

US Nationwide distribution.

What's affected?

Product
GE HealthCare OEC 9900 Elite C-arm Systems.
Lot code
GTIN: 00840682114349

Additional details

GTIN: 00840682114349

What should I do?

Recommended action

Class II recall. FDA Mandated

View original FDA notice →

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