FDA Device recall Z-0763-2016
Mavig Monitor Suspension System, Model GD60, contained in the following Fluoroscopic imaging systems: Advantx LCV+, Advantx LCN+, Advantx L…
- FDA Device
- Class II
- terminated
- Published 2016-02-17
On 2016-02-17 the FDA classified a Class II recall of Mavig Monitor Suspension System, Model GD60, contained in the following Fluoroscopic imaging systems: Advantx LCV+, Advantx LCN+, Advantx L… by Ge Medical Systems, citing GE Healthcare has recently become aware of a reported incident in which a Mavig suspension arm with monitor assembly fell to the floor.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0763-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-12-18 |
| Published | 2016-02-17 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ge Medical Systems |
| Distribution | US |
Product
Mavig Monitor Suspension System, Model GD60, contained in the following Fluoroscopic imaging systems: Advantx LCV+, Advantx LCN+, Advantx LCLP+, Advantx LCA, INNOVA 2000, INNOVA 4100, INNOVA 3100, INNOVA 3131IQ, INNOVA 2121IQ, INNOVA 2100IQ, INNOVA 3100IQ, and INNOVA 4100IQ
Reason
GE Healthcare has recently become aware of a reported incident in which a Mavig suspension arm with monitor assembly fell to the floor.
Identifiers
| code_info | Mfg Lot or Serial #/System ID, 1003/219326IN41, 20116/573632CRA, 30173/229434INNOV, 9110080/502587LAB4, 40410078/904276…Mfg Lot or Serial #/System ID, 1003/219326IN41, 20116/573632CRA, 30173/229434INNOV, 9110080/502587LAB4, 40410078/904276SP, 50410007/703689LCA2, 100300002/315448RM2, 104100042/650369SV5, 104100047/810342A41, 104100051/573632CRC1, 104100057/843674INNOVA, 106100046/603669ELCV, 110300023/315448RM1, 110310015/724656ANG, 110420162/251435I12, 120310008/804285CATH2, 123100037/617789IN1, 204110049/513861INNOVA, 204110065/623848LAB1, 304110059/908522CATH2, 304110070/519663INNOVA2, 304110071/850494WSP1, 404110063/903CSM4100, 404110077/808547QCV1A, 404110079/985867INNOVA2, 504110085/5094744100, 704120114/904202SP1, 704120117/619340VA8, 909110081/570969CATH, 1003100012/972335LIB, 1103100019/904202CATH2, 1103100026/315448RM3, 1104120128/812283IN20, 1203100022/702616INNOVA, 1203100032/515263IL4100, 1204130176/412623LAB3, 1204130198/918744JC4100, 1204930184/803329CL31, 000000007U0099/083016802100337, 00000007C20164/2706080, 00000007C20229/0835160022, 00000007C20367/MA1251VA01, 00000007C20369/00065VAS0 |
|---|
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-0763-2016%22
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