FDA Device recall Z-1706-2016
GE Healthcare, Discovery IGS 730
- FDA Device
- Class II
- terminated
- Published 2016-06-01
On 2016-06-01 the FDA classified a Class II recall of GE Healthcare, Discovery IGS 730 by Ge Medical Systems, citing potential non-recoverable loss of image acquisition. The affected Discovery systems may experience multiple X-Ray abort errors before or during a real-time fluoroscopic Interventi….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1706-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-04-15 |
| Published | 2016-06-01 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ge Medical Systems |
| Distribution | US |
Product
GE Healthcare, Discovery IGS 730. Indicated for use in generating fluoroscopic and rotational images of human anatomy.
Reason
Potential non-recoverable loss of image acquisition. The affected Discovery systems may experience multiple X-Ray abort errors before or during a real-time fluoroscopic Interventional procedure.
Identifiers
| code_info | Mfg Lot or Serial # System ID 664365BU4 804828CATH4 669085BU3 573815D730 668484BU9 714FVDISC 672437BU1 775770CATHLA…Mfg Lot or Serial # System ID 664365BU4 804828CATH4 669085BU3 573815D730 668484BU9 714FVDISC 672437BU1 775770CATHLAB3 0000HXF3001331 801714DIS730 00000632172BU3 203694IGS730 00000633128BU4 309624FT6 00000633831BU3 619532DISCOVERY 00000630288BU9 303426IR 0000HXF3001333 949250DISC730 00000637023BU3 214345IGS730 0000HXE9001300 650723SC1 00000646169BU3 330375HOR 00000638611BU4 414649DIS1 00000646917BU5 720854IGS730 00000614688BU0 610954OR1 00000622054BU5 423778DISC 646007BU5 206VMDISCOVERY1 00000637724BU6 281BAYIGS730 Not Avaialble GON4345699 Not Avaialble GON4110095 Not Avaialble DZ1104VA03 00000661681BU7 030078RX05 00000651337BU8 190059RX30 00000659126BU7 210060RX14 0000HXE9001292 613722D730 00000650197BU7 082416040061 00000653093BU5 082416040069 00000668482BU3 082416040074 Not Avaialble 082416060019 00000653092BU7 082416100080 00000651999BU5 082416120043 Not Avaialble 082416200019 00000618688BU6 M54866AG1 00000614687BU2 A4185526 0000013A2A0001 M404802 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1706-2016%22
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