NeuroLogica recalls HS70A ultrasound systems with specific versions and serial numbers due to potential probe overheating when reducing Doppler Sample Volume settings in Doppler Only mode.
There is a potential for probes overheating when decreasing the Doppler SV (Sample Volume) size value set by the user in the Doppler Only mode.
NeuroLogica is recalling specific versions of their HS70A Diagnostic Ultrasound System because users may cause probes to overheat by decreasing the Doppler Sample Volume setting in Doppler Only mode. This could lead to device damage or injury if not addressed.
When users decrease the Doppler Sample Volume (SV) value in Doppler Only mode, the probes can overheat. This overheating may cause device damage or potential injury to the user or patient if the probe becomes too hot.
Healthcare professionals using NeuroLogica HS70A ultrasound systems with the listed software versions and serial numbers are most at risk. Patients using these systems may also be affected if the probe overheats.
Check your HS70A ultrasound system's software version (2.01.00 to 2.01.06 or 1.00.06 to 1.00.12) and serial numbers listed in the recall notice. The recall includes specific serial numbers starting with S1C0M3HK or S15NM3HK.
Review your HS70A ultrasound system's software version to see if it matches the recalled versions (2.01.00 to 2.01.06 or 1.00.06 to 1.00.12).
Confirm your system's serial number is listed in the provided recall list (e.g., S1C0M3HK300004A, S1C0M3HK400005Z, etc.).
The recall is due to a potential risk of ultrasound probes overheating when users decrease the Doppler Sample Volume setting in Doppler Only mode.
Check your software version and serial number against the list provided in the recall notice to determine if your system is affected.
The recall record does not specify a remedy or fix for this issue.
We’ve drafted a message you can send NeuroLogica to request your refund or repair — edit it as you like.
Subject: Recall Z-2275-2019 — NeuroLogica NeuroLogica Hello, I own a NeuroLogica that is covered by recall Z-2275-2019 from NeuroLogica. 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.
