GE HealthCare OEC 9800.
FDA device recall Z-2341-2025 · posted 2025-08-22 · Open, Classified
Recall details
- Recalling firm
- GE Medical Systems, LLC
- Reason for recall
- 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.
- Action taken
- GE HealthCare will send a customer letter providing safety instructions as an immediate mitigation, to communicate the risk of additional radiation and that the equipment should only be used by personnel properly trained and authorized in the use of ionizing radiation. A user should observe proper safety practices during equipment operation as required by the operator manual. GE HealthCare will correct all affected OEC 9800 and OEC 9900 Elite systems (28 units) by visually inspecting for the presence of lead shield tape on the collimator cover and replacing the collimator cover if it is found non-compliant, at no cost to the customer.
- Root cause
- Radiation Control for Health and Safety Act
- Status
- Open, Classified
- Product code
- OWB
- Distribution
- US Nationwide distribution.
- Date initiated
- 2025-07-02
- Date posted
- 2025-08-22
- Location
- Waukesha, WI
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| OEC 9800 PLUS (K132027) | Ge Oec Medical Systems, Inc. | 2014-05-01 |
| OEC(R) 9800, OEC(R) 9800 PLUS (K111551) | Ge Oec Medical Systems, Inc. | 2011-10-04 |
| OEC 9800 PLUS DIGITAL MOBILE IMAGING SYSTEM (K021049) | Ge Oec Medical Systems | 2002-04-17 |