Device recall: Discovery IGS 730 Interventional Fluoroscopic X-ray Systems
Class II FDA enforcement event 80177. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
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.
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
GE Medical Systems, SCS started this device recall on 29 Mar 2018. The firm address in the FDA record is in Buc. FDA put the recall in Class II. FDA event 80177 has 3 product records. The first FDA enforcement report date is 18 Jul 2018. The record gives the status Terminated, with the termination date 15 Jun 2021.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
US distribution: AR, CA, CA, FL, GA, IA, IL, NC, NH, NJ, NM, NY, PA, SC, TN, A,WI, WV. International Distribution: Argentina, Brazil, China, Colombia, Egypt, France, India, Indonesia, Iran, Italy,…
Recalling firm
GE Medical Systems, SCS, Buc, France.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
3 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-2386-2018 | Discovery IGS 730 Interventional Fluoroscopic X-ray Systems | 102 devices total | Class II | Terminated | 18 Jul 2018 |
| Z-2387-2018 | Innova IGS 630/520/530/540 Interventional Fluoroscopic X-ray Systems | 102 devices total | Class II | Terminated | 18 Jul 2018 |
| Z-2388-2018 | Discovery IGS 740 Interventional Fluoroscopic X-ray Systems | 102 devices total | Class II | Terminated | 18 Jul 2018 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Device events that started in 2018
- 1,074
- Share of these events in Class II
- 92%
- Product records in this event
- 3Median of the firm: 1
- Events of the firm on the register
- 5
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 8 May 2026 | GE Healthcare AW Server 3.2 ext.6.5; Radiological Image Processing System | Device | Class II | 1 |
| 5 Sep 2025 | AW Server 2.0, AW Server 3.0, AW Server 3.1, AW Server 3.2 | Device | Class II | 1 |
| 18 Mar 2024 | GE Healthcare Innova IGS 5, computed tomography x-ray system | Device | Class II | 7 |
| 26 Dec 2023 | Senographe Pristina | Device | Class II | 1 |
Official channels
- FDA enforcement report Z-2386-2018The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA MedWatchThe FDA safety reporting program for drugs and medical devices.
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Cite this page
Recall Register. FDA enforcement event 80177. https://recallregister.com/fda/ii/80177/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA device enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
US distribution: AR, CA, CA, FL, GA, IA, IL, NC, NH, NJ, NM, NY, PA, SC, TN, A,WI, WV. International Distribution: Argentina, Brazil, China, Colombia, Egypt, France, India, Indonesia, Iran, Italy,…
- What quantity of product is in FDA event 80177?
- The event has 3 product records. The first record gives this quantity:
102 devices total
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many device recalls of 2018 have the same class?
- 92% of the 1,074 device events that started in 2018 are in Class II.