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Terminated

Quantum Pump Console

FDA Recall Z-2238-2019 · Posted 2019-08-23

Recalling FirmSpectrum Medical Ltd.
Recall StatusTerminated
Product CodeDTQ
Date Initiated2019-05-29
Date Terminated2020-08-21
Product Quantity108 units (8 US, 100 OUS)

Reason for Recall

Potential for Quantum Pump Console, part of the Quantum Perfusion Systems, to unexpectedly shut down while in use.

Firm Action

Spectrum Medical notified customers on about 05/29/2019 via "URGENT FIELD SAFETY CORRECTION" letter. Customers were informed that Spectrum Medical is in the process of installing the most recent software update v6.2.3.16 to the Quantum Perfusion Systems, (Quantum Pump Console). This software update corrects an error that could potentially lead to power loss. All Quantum Perfusion Systems are in scope of this issue. Customers were instructed to be aware that user intervention may be necessary with continued use before the software update, assure that all users receive notice of this issue, confirm receipt of the Urgent Medical Device Correction by returning the customer response form, and a Spectrum Medical service team will contact each customer and arrange a time and date to update the systems with the most recent software update. Additionally, customers were instructed to notify all relevant personnel and to customers if the devices have been further distributed.

Root Cause

Software design

Distribution Pattern

US distribution to NY, OH, VA, WA. International distribution to the Netherlands.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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