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O560 to D600 Upgrade 5607000Recalls & reported problems

GE Medical Systems, L.L.C. · Optima 560 Hardware Upgrade Collector, Manufacturing Make Assembly, Covers Plus Labels · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

  1. Jun 2, 2022Class IIOpen, Classified

    As a result of unclear guidance in the service manual, the table can drop during a specific service activity if the wrong screws are removed by the service personnel without the appropriate table supports in place resulting in injury to service personnel.

    Z-1511-2022 · Root cause: Error in labeling · Recall details · FDA record ↗

Other System, tomography, computed, emission devices

All System, tomography, computed, emission devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page