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FDA Medical Device Recalls (openFDA)

Terumo Cardiovascular Systems Corporation: Terumo Capiox NX19 Oxygenator With Reservoir (West Orientation) P/N: 3CX*NX19RW

Recall number
Z-2102-2019
Recalling firm
Terumo Cardiovascular Systems Corporation
Product
Terumo Capiox NX19 Oxygenator With Reservoir (West Orientation) P/N: 3CX*NX19RW
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
52units
Distribution
MI Foreign: Japan, Belgium
Lot, serial or model codes
Lot Numbers: XAl 1, XA28, XC07
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

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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

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