FDA Device recall Z-1798-2025
Product Name: Ingenia Ambition S
- FDA Device
- Class II
- ongoing
- Published 2025-05-28
On 2025-05-28 the FDA classified a Class II recall of Product Name: Ingenia Ambition S by Philips North America, citing potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1798-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-05-13 |
| Published | 2025-05-28 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips North America |
| Distribution | US |
Product
Product Name: Ingenia Ambition S; Model Numbers: (1) 781359, (2) 782108, (3) 782139;
Reason
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Identifiers
| code_info | Model Numbers: (1) 781359, (2) 782108, (3) 782139; UDI-DI: (1) 00884838090057, (2) 00884838009813, (3) 00884838098299;…Model Numbers: (1) 781359, (2) 782108, (3) 782139; UDI-DI: (1) 00884838090057, (2) 00884838009813, (3) 00884838098299; Serial Numbers: (1) 48001, 48005, 48009, 48011, 48014, 48016, 48023, 48033, 48034, 48043, 48045, 48047, 48122, 48154, 48160, 48167, 48173, 48178, 48179, 48180, 48242, 48275, 48285, (2) 48501, 48503, 48507, 48524, 48530, 48537, 48548, 48549, 48557, 48564, 48566, 48568, 48569, 48571, 48576, 48577, 48580, 48582, 48588, 48589, 48591, 48595, 48607, 48608, 48612, 48614, 48620, 48628, 48638, 48641, 48666, 48667, 48668, 48669, 48671, 48672, 48673, 48686, 48688, 48692, 48694, 48695, 48696, 48697, 48698, 48718, 48721, 48726, 48749, 48778, 48818, 48819, 48831, 48847, 48854, 48878, 48888, 48895, 48907, (3) 29000, 29003, 29005, 29006, 29008, 29009, 29010, 29011, 29012, 29013, 29014, 29015, 29016, 29017, 29018, 29019, 29020, 29021, 29022, 29023, 29025, 29026, 29027, 29029, 29030, 29031, 29032, 29033, 29034, 29035, 29038, 29039, 29040, 29042, 29043, 29045, 29046, 29047, 29048, 29049, |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1798-2025%22
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