Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software defect; programming errors in the blood flow...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Transonic Systems Inc directly.
Affected Products
Transonic Flow Probe, 8 mm, Catalog Number HQC8FMV -- Product Usage: to measure flow intra-operatively.
Quantity: Domestic: 5 units
Why Was This Recalled?
Software defect; programming errors in the blood flow probes EPROM. Transonic received several complaints from users indicating that when the flow probe is connected to a flow meter the meter reads Used Probe or Irrelevant Use Number.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Transonic Systems Inc
Transonic Systems Inc has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report