Z-0425-05

Bio Med Devices Patient Breathing Circuit Catalog Number: 8002A Labeled in part: ONE SET - SINGLE USE CATALOG...

Name: Z-0425-05 Bio Med Devices Patient Breathing Circuit Catalog Number: 8002A Labeled in part: ONE SET - SINGLE USE CATALOG...
Creator: Bio-Med Devices, Inc.
Published: 2004-12-06
License: https://open.fda.gov/license/

Bio-Med Devices, Inc. / initiated 2004-12-06 / Terminated

FDA source

Bio-Med Devices, Inc. began a recall of Bio Med Devices Patient Breathing Circuit Catalog Number: 8002A Labeled in part: ONE SET - SINGLE USE CATALOG NO. 8002A PATIENT BREATHING CIRCUIT... on 2004-12-06. The reason FDA records is "Adapters may be occluded potentially preventing inhalation". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0425-05
Status: Terminated
Initiated: 2004-12-06
Posted: 2005-01-29
Terminated: 2005-11-21
Recalling firm: Bio-Med Devices, Inc.
Product: Bio Med Devices Patient Breathing Circuit Catalog Number: 8002A Labeled in part: ONE SET - SINGLE USE CATALOG NO. 8002A PATIENT BREATHING CIRCUIT =-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-= CONTENTS: 1-PATIENT HOSE 22mmIDx42'' 1-PRESSURE GAGE LINE 1-PATIENT HOSE 22mmIDx6'' 1-EXHALATION VALVE w/HOLDING ARM& COLLECTION HEAD 48'' w/CUFF 1/4''ID 1-ADULT PRESSURE TEE w/CUFF 1-EXHALATION VALVE LINE 1/8''IDx48'' 2-ADAPTERS 22mmx22mm
Product code: CBK Ventilator, Continuous, Facility Use
Reason for recall: Adapters may be occluded potentially preventing inhalation
FDA root cause: Other
Action: Bio-Med Devices issued recall notifcation by fax on 12/7/04. Accounts are requested to discontine use and return product. A Press Release issued to AP 12/8/04
Quantity in commerce: 58 cs
Distribution: Nationwide Forign: Canada, Greece, Japna, Israel, Saudi Arabia,
Product codes and lots: Lot Numbers: last 6 digits 09092204, 01092404, 05093004, 01100604 05100704, 02100804, 05101204, 01101804 09102804, 01110104, 09110404, 05110404 05110904, 05111104, 09111604, 09111804 09111904, 09112204, 09112404, 05120104

Product code CBK

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)