FDA Medical Device Recalls (openFDA)
CAS Medical Systems, Inc.: CASMED 500cc Unifusor with aneroid gauge and stopcock valve. Model: A803SGA . The letter A refers to a special quantity designator for a particular customer. The product is designed for use in rapid infusion,invasive pressure monitoring and with auto-transfusion devices.
- Recall number
- Z-0463-2009
- Recalling firm
- CAS Medical Systems, Inc.
- Product
- CASMED 500cc Unifusor with aneroid gauge and stopcock valve. Model: A803SGA . The letter A refers to a special quantity designator for a particular customer. The product is designed for use in rapid infusion,invasive pressure monitoring and with auto-transfusion devices.
- Status
- Terminated
- Initiated
- 2008-09-20
- Posted
- 2008-12-29
- Terminated
- 2010-08-05
- Reason
- Leaks: Infusion Cuffs may exhibit air leakage at the union of the tube and bag, and not maintain pressure. For further information, please contact the firm at 203-488-6056.
- Root cause
- Equipment maintenance
- Action
- CAS Medical Systems notified accounts by letter dated 9/19/08 requesting return and sub-recall be conducted to their accounts. The letter was entitled "UNIFUSOR(R) INFUSION CUFFS AND PRIVATE LABEL (CASMED-MANUFACTURED) INFUSION CUFFS *** URGENT PRODUCT CORRECTION NOTICE." For further information, please contact the firm at 203-488-6056.
- Quantity
- 19,440 pc
- Distribution
- Nationwide Foreign: Malaysia, Austria, Belgium, Czech Rep., France, Germany, Greece, Italy, Norway, Spain, Sweden, Switzerland and the UK.
- Lot, serial or model codes
- Lot Numbers: 22810808, 24740908, 24750908, 25470908, 25480908, 27271108, 27281108, 31181308, 34511608, 40072008, 41112108, and 41362108, 41802108, 42462208, 42482208, 43472308, 44772408, 44802408, 44812408, 46902508, 46962508, 48692608.
- 510(k) numbers
- ["K893519"]
- PMA numbers
- not on file
- Product code
- KZD
- Firm FEI
- 2244861
- Firm city
- Branford
- Firm state
- CT
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28