Bio-Med Devices, Inc. Bio Med Devices Patient Breathing Circuit Catalog Number: 80011 Labeled in part: '':PATIENT BREATHING CIRCUIT =-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-= CONTENTS: 1-PATIENT HOSE 22mmIDx42'' 1-PRESSURE GAGE LINE 3/16''IDx54'' 1-PATIENT HOSE 22mmIDx24'' 3-ADAPTERS 22mm x 22mm 1-PATIENT HOSE 22mmIDx6'' 1-ADULT PRESSURE TEE 1-EXHALATION VALVE w/HOLDING ARM& 1-TEMPERATURE ADAP Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Bio Med Devices Patient Breathing Circuit Catalog Number: 80011 Labeled in part: '':PATIENT BREATHING CIRCUIT =-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-= CONTENTS: 1-PATIENT HOSE 22mmIDx42'' 1-PRESSURE GAGE LINE 3/16''IDx54'' 1-PATIENT HOSE 22mmIDx24'' 3-ADAPTERS 22mm x 22mm 1-PATIENT HOSE 22mmIDx6'' 1-ADULT PRESSURE TEE 1-EXHALATION VALVE w/HOLDING ARM& 1-TEMPERATURE ADAP
Brand
Bio-Med Devices, Inc.
Lot Codes / Batch Numbers
Lot Numbers: Last 6 digits 01092304, 01092404, 01092804, 01092904, 01093004, 01100504, 01100604, 01100704 01100804, 01101104, 01101204, 01101404 01101504, 02101804, 01101904, 01102004 01102104, 01102204, 01102504, 05102504 01102604, 01102804, 01102904, 01110104 01110204, 01110504, 09111004, 01111104 05111204, 09111604, 01111704, 01111904 01112204, 09112404, 09113004, 09120204
Products Sold
Lot Numbers: Last 6 digits 01092304, 01092404, 01092804, 01092904, 01093004, 01100504, 01100604, 01100704 01100804, 01101104, 01101204, 01101404 01101504, 02101804, 01101904, 01102004 01102104, 01102204, 01102504, 05102504 01102604, 01102804, 01102904, 01110104 01110204, 01110504, 09111004, 01111104 05111204, 09111604, 01111704, 01111904 01112204, 09112404, 09113004, 09120204
Bio-Med Devices, Inc. is recalling Bio Med Devices Patient Breathing Circuit Catalog Number: 80011 Labeled in part: '':PATIENT BREAT due to Adapters may be occluded potentially preventing inhalation. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Adapters may be occluded potentially preventing inhalation
Recommended Action
Per FDA guidance
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
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026