FDA Medical Device Recalls (openFDA)
Terumo Cardiovascular Systems Corp: Terumo L Series 1863 type arterial perfusion cannulae, straight open tip, 1/4'' connector, arterial cannula, 12 FR, 17.5 cm (7'') long; Catalog no. L7351.
- Recall number
- Z-0544-2007
- Recalling firm
- Terumo Cardiovascular Systems Corp
- Product
- Terumo L Series 1863 type arterial perfusion cannulae, straight open tip, 1/4'' connector, arterial cannula, 12 FR, 17.5 cm (7'') long; Catalog no. L7351.
- Status
- Terminated
- Initiated
- 2006-12-07
- Posted
- 2007-02-27
- Terminated
- 2007-12-05
- Reason
- The cannula connector is an incorrect size: It is actually 1/4" by 3/8" instead of the correct 1/4" by 1/4".
- Root cause
- Other
- Action
- Consignee was notified via telephone on 12/7/06 and returned the product.
- Quantity
- 10
- Distribution
- Pennsylvania.
- Lot, serial or model codes
- Lot 2119905, exp. October 2009.
- 510(k) numbers
- ["K930620"]
- PMA numbers
- not on file
- Product code
- DWF
- Firm FEI
- 1828100
- Firm city
- Ann Arbor
- Firm state
- MI
- 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