Transonic Systems Inc: Medical Device Recall in 2015 - (Recall #: Z-2726-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Transonic Flow Probe, 2 mm, Catalog Number HQD2FMC -- Product Usage: to measure flow intra-operatively.

Product Classification:

Class II

Date Initiated: July 27, 2015

Date Posted: September 9, 2015

Recall Number: Z-2726-2015

Event ID: 71907

Reason for Recall:

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.

Status: Terminated

Product Quantity: Domestic: 8 units, foreign: 11 units

Code Information:

Serial Numbers: HQD2FMC2797, HQD2FMC2873, HQD2FMC2874, HQD2FMC2875, HQD2FMC2876, HQD2FMC2877, HQD2FMC2878, HQD2FMC2879, HQD2FMC2880, HQD2FMC2881, HQD2FMC2882, HQD2FMC2883, HQD2FMC2884, HQD2FMC2885, HQD2FMC2886, HQD2FMC2888, HQD2FMC2889, HQD2FMC2890, HQD2FMC2908

Distribution Pattern:

Worldwide Distribution - US Nationwide and the countries of: Canada, Japan, Russia and The Netherlands.

Voluntary or Mandated:

Voluntary: Firm initiated