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Allia IGS 5 Pulse angiographic X-ray system

Lot codes and dates: UDI-DI00195278719263
Serial Numbers
150 of 150 codes
M2-23-039
M2-23-056
M2-24-004
M2-24-019
M2-24-020
M2-24-025
M2-24-030
M2-24-031
M2-24-032
M2-24-033
M2-24-034
M2-24-037
M2-24-038
M2-24-039
M2-24-040
M2-24-046
M2-24-057
M2-24-062
M2-24-064
M2-24-066
M2-24-069
M2-24-071
M2-24-077
M2-24-078
M2-24-080
M2-24-083
M2-25-003
M2-25-004
M2-25-005
M2-25-011
M2-25-013
M2-25-015
M2-25-017
M2-25-019
M2-25-023
M2-25-024
M2-25-025
M2-25-026
M2-25-028
M2-25-032
M2-25-036
M2-25-037
M2-25-039
M2-25-040
M2-25-041
M2-25-042
M2-25-043
M2-25-046
M2-25-048
M2-25-049
M2-25-056
M2-25-057
M2-25-058
M2-25-062
M2-25-065
M2-25-067
M2-25-072
M2-25-074
M2-25-077
M2-25-078
Amount recalled: 121 units

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

Nationwide

Why it was recalled

GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.

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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Other recalls from GE Medical Systems, LLC

36 in total.

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