FDA Device recall Z-1551-2013
GE Healthcare, PET VCAR. PET VCAR application software is affected if installed on any of the following versions of the Advantage Workstati…
- FDA Device
- Class II
- terminated
- Published 2013-06-26
On 2013-06-26 the FDA classified a Class II recall of GE Healthcare, PET VCAR. PET VCAR application software is affected if installed on any of the following versions of the Advantage Workstati… by Ge Healthcare, citing GE Healthcare has recently become aware of a potential safety issue with respect to the automated PERCIST response criteria calculation applied in the PET VCAR application on Adva….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1551-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-05-09 |
| Published | 2013-06-26 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ge Healthcare |
| Distribution | CA, CO, CT, FL, GA, IL, NC, NY, OH, TX, VA, WI, WV |
Product
GE Healthcare, PET VCAR. PET VCAR application software is affected if installed on any of the following versions of the Advantage Workstation and AW Server: Advantage Workstation 4.6, Volume Share 5 enhanced vxtl.11.3, vxtl.11.3 ext1, or vxtl.11.3 ext2 AW Server 2.0, Volume Share 5 enhanced vxtl.11.3, vxtl.11.3 ext1, or vxtl.11.3 ext2 PET VCAR (Volume Computer Assisted Reading) is a PET/CT software package which can be used by the clinician to assist in diagnosis, staging, treatment planning and monitoring treatment response.
Reason
GE Healthcare has recently become aware of a potential safety issue with respect to the automated PERCIST response criteria calculation applied in the PET VCAR application on Advantage Workstation or AW Server.
Identifiers
| code_info | Mfg Lot or Serial # 00000L3A331FA4 00000L3A3318C4 0S804VCUPETAWS 00S804VCUPETAW 00000LE23E908A 00000LA707B8CD 00…Mfg Lot or Serial # 00000L3A331FA4 00000L3A3318C4 0S804VCUPETAWS 00S804VCUPETAW 00000LE23E908A 00000LA707B8CD 0000S704783AWS 00000L3AB67847 000D1L3AB67847 00000LA70D61FE 0000G297117701 00000LFB44C088 00000LA70D6257 00000L2E5D97AC 00000LA704C3E7 00000L021DFE17 00000L97BF02A6 00000L3AA73A5B 00000LA70AB28E 00000L3AB4D639 00000L3AB501ED 00000L3AA80D28 00000L3AB4D6CC 00000L3AB50126 SNYPHAWSERVER2 00000X12335005 00000LAEDF9764 000S704783HDCT 0D1S704783HDCT SSENTARAPETDST 00000LB8CDB088 00000LA70CF2BD 00S681342AWONC 00000L97BD2680 0S856247PETUPS 00000L3AAD0E3F 00000L3A6AB2B5 00000L3A3D0C38 00000LA7053E64 00000LA7053E11 00000H12361003 00000H12361004 0000AD13018005 00000E12291003 00000E12291004 0000AV12212003 0000AV12212004 0000AV12213001 0000AV12213002 00000R12268002 00000R12268003 00000N12226004 00000N12226005 00000L3A330899 00000L3A87FE86 00000L3A86843C 00000L3A3305A1 00000LA713783D 00000LA712A01B 00000LA7142C7C SCT428868CN4AW 000 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1551-2013%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.