FDA Medical Device Recalls (openFDA)
Instrumentation Industries Inc: Flexible Support Arm Assembly. Breathing Tube Support. Catalog number BE 122-30
- Recall number
- Z-0427-06
- Recalling firm
- Instrumentation Industries Inc
- Product
- Flexible Support Arm Assembly. Breathing Tube Support. Catalog number BE 122-30
- Status
- Terminated
- Initiated
- 2005-10-14
- Posted
- 2006-01-24
- Terminated
- 2006-05-09
- Reason
- potential for the flexible tube portion of the assembly to become brittle and break
- Root cause
- Other
- Action
- 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.
- Quantity
- 22 units
- Distribution
- The products were shipped to medical facilities in FL, NY, and WV.
- Lot, serial or model codes
- Lot numbers PO902505 and PO900805
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- JAY
- Firm FEI
- 2518436
- Firm city
- Bethel Park
- Firm state
- PA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28