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FDA · FDA event 94988 · Posted Aug 16, 2024
The Spectrum WBM may fail to auto-document infusion status information back to the hospital's Electronic Medical Record (EMR) system. This software issue only impacts customers where the Spectrum V8 or Spectrum IQ infusion system is integrated with the hospital s EMR system.
The official notice takes precedence over this summary. Talk to your clinician before changing prescribed therapy.
| Model | Description | Lot / serial range | Manufactured | Status |
|---|---|---|---|---|
| Z-2581-2024 | Z-2581-2024 | Pump GTIN 00085412498683; All serial numbers with radio software versions 22D28, 22D29, and 22D30 | Not provided in the normalized record | Ongoing |
| Z-2582-2024 | Z-2582-2024 | Pump UDI/DI GTIN 00085412498683; All serial numbers with radio software versions 22D28, 22D29, and 22D30 | Not provided in the normalized record | Ongoing |
Jul 17, 2024
Recall initiated
Date recorded by the FDA.
Aug 16, 2024
Posted by FDA
The recall event appeared in the FDA source.
Oct 8, 2026
Last checked
MedWatcher last reconciled this record with the openFDA export.