Spectrum Medical recalls
Spectrum Medical has 7 recalls on record with the FDA and USDA, the earliest in 2019 and the latest reported on 7 Oct 2026. 5 are still ongoing. 2 were reported in the last 12 months. The most frequent reason is packaging defects.
Total recalls7since 2019
Last 12 months2reported
Class I114% of total
Ongoing5latest 7 Oct 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 1 14%Class II 6 86%Class III 0 0%
Why spectrum medical is recalled
Product types
By year
Ongoing spectrum medical recalls
5 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Quantum PureFlow Standard Heat Exchanger High Flow 3/8 recalled | Spectrum Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Quantum PureFlow Standard Heat Exchanger High Flow 3/8 recalled | Spectrum Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Quantum Informatics - Vision / Live Vue Monitor recalled | Spectrum Medical | Device Malfunction | 38 states |
| Device | CLASS II | Quantum Informatics - Viper Monitor, Physiological, Patient recalled | Spectrum Medical | Device Malfunction | 38 states |
| Device | CLASS II | Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type recalled | Spectrum Medical | Packaging Defects | Nationwide |
All spectrum medical recalls, newest first
7 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Quantum PureFlow Standard Heat Exchanger High Flow 3/8 recalled | Spectrum Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Quantum PureFlow Standard Heat Exchanger High Flow 3/8 recalled | Spectrum Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Quantum Informatics - Vision / Live Vue Monitor recalled | Spectrum Medical | Device Malfunction | 38 states |
| Device | CLASS II | Quantum Informatics - Viper Monitor, Physiological, Patient recalled | Spectrum Medical | Device Malfunction | 38 states |
| Device | CLASS II | Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type recalled | Spectrum Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Quantum Perfusion Systems for CPB recalled by Spectrum Medical | Spectrum Medical | Other | Nationwide |
| Device | CLASS I | Quantum Pump Console recalled by Spectrum Medical | Spectrum Medical | Other | 4 states |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.