Z-0427-06

Flexible Support Arm Assembly. Breathing Tube Support. Catalog number BE 122-30

Name: Z-0427-06 Flexible Support Arm Assembly. Breathing Tube Support. Catalog number BE 122-30
Creator: Instrumentation Industries Inc
Published: 2005-10-14
License: https://open.fda.gov/license/

Instrumentation Industries, Incorporated / initiated 2005-10-14 / Terminated

FDA source

Instrumentation Industries Inc began a recall of Flexible Support Arm Assembly. Breathing Tube Support. Catalog number BE 122-30 on 2005-10-14. The reason FDA records is "potential for the flexible tube portion of the assembly to become brittle and break". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0427-06
Status: Terminated
Initiated: 2005-10-14
Posted: 2006-01-24
Terminated: 2006-05-09
Recalling firm: Instrumentation Industries, Incorporated
Product: Flexible Support Arm Assembly. Breathing Tube Support. Catalog number BE 122-30
Product code: JAY Support, Breathing Tube
Reason for recall: potential for the flexible tube portion of the assembly to become brittle and break
FDA 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 in commerce: 22 units
Distribution: The products were shipped to medical facilities in FL, NY, and WV.
Product codes and lots: Lot numbers PO902505 and PO900805

Product code JAY

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)