Flexible Support Arm Assembly. Breathing Tube Support. Catalog number BE 122-30
FDA device recall Z-0427-06 · posted 2006-01-24 · Terminated
Recall details
- Recalling firm
- Instrumentation Industries Inc
- Reason for recall
- potential for the flexible tube portion of the assembly to become brittle and break
- Action taken
- All customers (and/or end-users) were notified on October 14 and 17, 2005 by telephone. Formal notification letters were sent (certified) to each customer (and/or end-user) on October 17 and 18, 2005.
- Root cause
- Other
- Status
- Terminated
- Product code
- JAY
- Quantity affected
- 22 units
- Distribution
- The products were shipped to medical facilities in FL, NY, and WV.
- Date initiated
- 2005-10-14
- Date posted
- 2006-01-24
- Date terminated
- 2006-05-09
- Location
- Bethel Park, PA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.