QFC1631, QFC1683, QFC1685 Quick Connects for use with Fujinon gastrointestinal endoscopes, for use with the STERIS SYSTE
FDA device recall Z-0724-03 · posted 2003-04-16 · Terminated
Recall details
- Recalling firm
- Steris Corp
- Reason for recall
- The defective device may restrict the flow of sterilant to the attached endoscope and affect the sterilization process of the scope.
- Action taken
- The firm contacted their affected consignees by telephone and letter on 3/20/2003.
- Root cause
- Other
- Status
- Terminated
- Product code
- MLR
- Quantity affected
- 46
- Distribution
- The devices were shipped to hospitals located in ME, NB, CA, IL, NJ, OH, IL, TX, MA, GA, MO, NC, and FL.
- Date initiated
- 2003-03-20
- Date posted
- 2003-04-16
- Date terminated
- 2004-02-05
- Location
- Mentor, OH
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.