FDA Device recall Z-1964-2019
Refurbish RIC5-9-D Probe ROHS compliant Ultrasound Probe RIC5-9-D
- FDA Device
- Class II
- terminated
- Published 2019-07-24
On 2019-07-24 the FDA classified a Class II recall of Refurbish RIC5-9-D Probe ROHS compliant Ultrasound Probe RIC5-9-D by Ge Healthcare, citing potential for a transducer mis-alignment in certain transvaginal probes.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1964-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-07-02 |
| Published | 2019-07-24 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Ge Healthcare |
| Distribution | TX |
Product
Refurbish RIC5-9-D Probe ROHS compliant Ultrasound Probe RIC5-9-D
Reason
Potential for a transducer mis-alignment in certain transvaginal probes.
Identifiers
| code_info | Model KTZ303987-R - Serial Number (UDI Number): 226914KR0 (01008406821084301118032721226914KR0), 198026KR7 (Not Availab…Model KTZ303987-R - Serial Number (UDI Number): 226914KR0 (01008406821084301118032721226914KR0), 198026KR7 (Not Available), 220616KR7 (01008406821084301117091521220616KR7), 205375KR9 (01008406821085531116071121205375KR9) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1964-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.