Spectrum Medical recalls Quantum Pump Consoles with software version 6.2.1.9 due to potential unexpected shutdowns while in use. Affected units have specific serial numbers listed in the recall notice.
Potential for Quantum Pump Console, part of the Quantum Perfusion Systems, to unexpectedly shut down while in use.
Spectrum Medical is recalling Quantum Pump Consoles that are part of the Quantum Perfusion Systems. These devices may unexpectedly shut down while being used, which could disrupt medical treatment. Affected units have specific serial numbers listed in the recall notice.
The Quantum Pump Console may unexpectedly shut down while in use, potentially interrupting medical treatment. This could lead to complications for patients relying on the device for critical care.
Patients using the Quantum Pump Console for medical treatment are most at risk. The recall affects specific units with software version 6.2.1.9 and listed serial numbers.
Check if your Quantum Pump Console has software version 6.2.1.9. Affected units have specific serial numbers listed in the recall notice, including PH1000005 through PH1000940.
Verify your Quantum Pump Console's software version; affected units have version 6.2.1.9.
Reach out to Spectrum Medical for assistance with the recall and to confirm if your unit is affected.
The Quantum Pump Console may unexpectedly shut down while in use, which could disrupt medical treatment for patients.
Software version 6.2.1.9 is affected.
Check your Quantum Pump Console's serial number against the list of affected units provided in the recall notice.
We’ve drafted a message you can send Spectrum Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2238-2019 — Spectrum Medical Spectrum Medical Hello, I own a Spectrum Medical that is covered by recall Z-2238-2019 from Spectrum Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.