Reported Jul 18, 2018 · Terminated
Discovery IGS 730 Interventional Fluoroscopic X-ray Systems
GE Medical Systems, SCS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: GE Medical Systems, SCS · 283 rue de la Miniere · Buc · N/A
Is this the product you have?
- Discovery IGS 730 Interventional Fluoroscopic X-ray Systems
- Lot codes and dates
- Model Number 5730890
- Serial Numbers (System ID)
00000D3-17-030 (904BHHCHY)00000D3-17-032 (083172440628)661327IGS730 (00000D3-18-001)GON4598369 (00000D3-18-004)082416140028 (00000D3-17-025)M4234253 (00000D3-17-028)YV3601 (00000D3-18-005)6073XR0058 (00000D3-17-031)
- Amount recalled
- 102 devices total
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
The Discovery IGS and Innova IGS systems may experience X-ray abort errors which could result in the loss of imaging mode before or during fluoroscopic use.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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