Axiom Aristos MX Solid State Flat Panel Digital Imager, Model number 5895003. The device is used for diagnostic X-ray im
FDA device recall Z-1795-2013 · posted 2013-07-24 · Terminated
Recall details
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Reason for recall
- Siemens issued a Field Safety Notice about the potential hazard to patients or operators when using the function "table top float" of the AXIOM Aristos MX. When repositioning a patient lying on the table top and releasing the table top, it is possible that the fingers of the patient or operator are between the table top and the detector tray and if the table top is moved, the fingers can be squee
- Action taken
- On 6/5/13, consignees were notified by letter of a "Field Safety Notice" and received instructions about how to avoid the potential risk of this issue while using the device. Siemens also rolled out a modification of AXIOM Aristos MX that will avoid these potential injuries in the future.
- Root cause
- Device Design
- Status
- Terminated
- Product code
- MQB
- Quantity affected
- 401
- Distribution
- Nationwide Distribution.
- Date initiated
- 2013-06-05
- Date posted
- 2013-07-24
- Date terminated
- 2015-02-24
- Location
- Malvern, PA
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| THORAX FD AND MULTIX FD (K983732) | Siemens Medical Solutions USA, Inc. | 1999-04-21 |