Bio Med Devices Patient Breathing Circuit Catalog Number: 8002A-7 Labeled in part: ONE SET - SINGLE USE ATALOG NO. 8002A
FDA device recall Z-0426-05 · posted 2005-01-29 · Terminated
Recall details
- Recalling firm
- Bio-Med Devices, Inc.
- Reason for recall
- Adapters may be occluded potentially preventing inhalation
- Action taken
- 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
- Root cause
- Other
- Status
- Terminated
- Product code
- CBK
- Quantity affected
- 71 cs
- Distribution
- Nationwide Forign: Canada, Greece, Japna, Israel, Saudi Arabia,
- Date initiated
- 2004-12-06
- Date posted
- 2005-01-29
- Date terminated
- 2005-11-21
- Location
- Guilford, CT
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