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U.S. Department of Health and Human Services

Class 1 Device Recall BioMed Devices

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 Class 1 Device Recall BioMed Devicessee related information
Date Initiated by FirmDecember 06, 2004
Date PostedJanuary 29, 2005
Recall Status1 Terminated 3 on November 21, 2005
Recall NumberZ-0426-05
Recall Event ID 30580
Product Classification Ventilator, Continuous, Facility Use - Product Code CBK
ProductBio Med Devices Patient Breathing Circuit Catalog Number: 8002A-7 Labeled in part: ONE SET - SINGLE USE ATALOG NO. 8002A-7 PATIENT BREATHING CIRCUIT =-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-= CONTENTS: 1-PATIENT HOSE 22mmIDx60'' 1-EXHALATION VALVE LINE 1/8''IDx90'' 1-PATIENT HOSE 22mmIDx18'' 1-PATIENT HOSE 22mmIDx6'' 1-PRESSURE GAGE LINE 84'' w/CUFF 1/4''ID 1-EXHALATION VALVE w/HOLDING ARM& COLLECTION HEAD 1-ADULT PRESSURE TEE w/CUFF 3-ADAPTERS 22mmx22mm
Code Information Lot Numbers: 05092304, 01092804, 01100104, 05100504 01100604, 05100704, 05101204, 01101304 05102104, 01102504, 01102604, 09102704 09102804, 09110404, 01110404, 09110504 09110904, 02111004, 09111104, 09111204 09111504, 09112304, 09112904, 09113004 09120104 
FEI Number 3003952420
Recalling Firm/
Manufacturer		 Bio-Med Devices, Inc.
1445 Boston Post Road
Guilford CT 06437-4338
For Additional Information ContactKen Close
203-458-0202
Manufacturer Reason
for Recall		Adapters may be occluded potentially preventing inhalation
FDA Determined
Cause 2		Other
ActionBio-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 Commerce71 cs
DistributionNationwide Forign: Canada, Greece, Japna, Israel, Saudi Arabia,
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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