Skip to content

HarmonyAIR A-Series Suspension System (REF LAS52NC01)Recalls & reported problems

Steris Corporation · The A-Series Single Accessory Mount, 67-Inch Arm, 13-Inch Drop Tube, No Controller is used with the HarmonyAIR A-Series Suspension System. · Class 1

2 open recalls name 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
2

Summary

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

2 FDA recall records name this device's identifier, 2 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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. May 15, 2026Open, Classified

    There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads.

    Z-2448-2026 · Root cause: Process change control · FDA record ↗

  2. May 15, 2026Open, Classified

    The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.

    Z-2449-2026 · Root cause: Material/Component Contamination · FDA record ↗

Other TABLE, OPERATING-ROOM, AC-POWERED devices

All TABLE, OPERATING-ROOM, AC-POWERED devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.