Device recall

Z-0724-03: QFC1631, QFC1683, QFC1685 Quick Connects for use with Fujinon gastrointestinal…

FDA device recall · Class II · Steris Corp

Key facts

Recall number (Z-number) Z-0724-03
Recall event 25946
Product QFC1631, QFC1683, QFC1685 Quick Connects for use with Fujinon gastrointestinal endoscopes, for use with the STERIS SYSTEM I Processor and the C1160 Universal Flexible Processing Tray. The QFC1631 is for Fujinon 450/485 Series Video Gastroscopes; The QFC1683 is for Fujinon EC-450LP Colonoscopes; The…
Product code MLR
Recalling firm Steris Corp
Recall class Class II
Status Terminated
Termination date Feb 5, 2004
510(k) numbers K875280
FEI number 1527821

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

Browse all FDA device recalls (products)