FDA Medical Device Recalls (openFDA)
Terumo Cardiovascular Systems Corporation: Terumo Capiox NX19 Oxygenator (East Orientation), P/N: CXOT280 Exported only to Japan for inclusion into convenience kits that are sold only within the Japanese market
- Recall number
- Z-2103-2019
- Recalling firm
- Terumo Cardiovascular Systems Corporation
- Product
- Terumo Capiox NX19 Oxygenator (East Orientation), P/N: CXOT280 Exported only to Japan for inclusion into convenience kits that are sold only within the Japanese market
- Status
- Terminated
- Initiated
- 2019-06-14
- Posted
- not on file
- Terminated
- 2020-06-11
- Reason
- Capiox NX19 Oxygenator may contain a non-functioning arterial thermistor component
- Root cause
- Process control
- Action
- Terumo issued Urgent Medical Device Notification letter dated June 13 2019 via FedEx mailing executed on 6/14/2019 advising of the problem, health risk and action to take: Terumo CVS advises users to remove all affected product from inventory and return unused product to Terumo CVS following the instructions provided in this notice. Questions or concerns: Terumo CVS Customer Service: 1.800.521.2818 Monday Friday, 8 a.m. 6 p.m. ET Terumo Recall Fax: 1.410.392.7183 Terumo Recall Email: TCVSCustomerResponseElkton@terumomedical.com
- Quantity
- 78 units
- Distribution
- MI Foreign: Japan, Belgium
- Lot, serial or model codes
- Lot Numbers: XA28, XC12, XC25, XD05, XD27
- 510(k) numbers
- ["K180950"]
- PMA numbers
- not on file
- Product code
- DTZ
- Firm FEI
- 3000204839
- Firm city
- Elkton
- Firm state
- MD
- 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