FDA Medical Device Recalls (openFDA)
Datascope Corporation: HemaCarotid Patch, Ultrathin, Collagen Coated Knitted Polyester Vascular Patch. Product Catalog Numbers: HEK06/75CPUT; HEK08/75CPUT; HEK14/75CPUT; HEK08/120CPUT; HEK10/75CPUT; HEK25/100CPUT; HEK12/75CPUT; HEK10/150CPUT.
- Recall number
- Z-0638-04
- Recalling firm
- Datascope Corporation
- Product
- HemaCarotid Patch, Ultrathin, Collagen Coated Knitted Polyester Vascular Patch. Product Catalog Numbers: HEK06/75CPUT; HEK08/75CPUT; HEK14/75CPUT; HEK08/120CPUT; HEK10/75CPUT; HEK25/100CPUT; HEK12/75CPUT; HEK10/150CPUT.
- Status
- Terminated
- Initiated
- 2003-12-30
- Posted
- 2004-07-20
- Terminated
- 2006-01-19
- Reason
- Water permeability of the patch is out of specification.
- Root cause
- Other
- Action
- Recall letters were sent to the customers via US Mail return receipt on 12/30/2003.
- Quantity
- 710 units
- Distribution
- The product has been shipped nationwide to 53 hospitals, 4 government hospitals, and 3 sales representatives.
- Lot, serial or model codes
- Lot Numbers: 03G03; 03H08; 03J25; 03G10; 03H28; 03K02; 03G17; 03J04; 03K09; 03G24; 03J11; 03K16; 03G31; 03J18; 03K23.
- 510(k) numbers
- ["K983819"]
- PMA numbers
- not on file
- Product code
- DSY
- Firm FEI
- 2221819
- Firm city
- Montvale
- Firm state
- NJ
- 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
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
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