The Recall Desk
HighFDA (Devices)·Z-2255-2012·Announced 2012-09-19

GE Healthcare Recalls Optima XR220amx Mobile X-Ray Units Due to Software Issue

GE Healthcare is recalling 254 Optima XR220amx mobile X-ray units in the US because a software defect allows exposures without displaying technique factors.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall is classified as FDA Class II and involves a risk-of-harm product (radiographic imaging) where the defect allows exposures without displaying technique factors, but no injuries or illnesses are reported in the source text.

Plain-English summary

GE Healthcare, LLC is recalling 254 Optima XR220amx mobile general purpose radiographic imaging units in the United States. The recall is due to a software issue that violates 21 CFR 1020.31(a). The affected units are identified by part numbers 5555000-3, 5555000-4, 5555000-5, and 5555000-6.

The software defect occurs after an image is taken. When a user selects and clears an additionally displayed screen, the system inhibit is also cleared. This allows the user to take an exposure without the technique factors being displayed. The FDA has classified this recall as Class II.

Healthcare facilities using these devices should contact GE Healthcare for instructions on how to resolve the issue. No specific instructions for end-users are provided in the source text, but the recall affects the safety and compliance of the imaging process.

The recalled product

Product
Optima XR220amx Mobile general purpose radiographic imaging of the human head and body.
Manufacturer
GE Healthcare, LLC
Category
Medical Device — Radiographic Imaging
Hazard
Affected units
254

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (4)

  • Part Numbers: 5555000-3
  • 5555000-4
  • 5555000-5
  • 5555000-6.

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 2 recalled by GE Healthcare, LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 2 products in this recall →

Related recalls

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