FDA Medical Device Recalls (openFDA)
Cook Incorporated: Vinyl Connecting Tube, Connecting Tube Reference Part Number/GPN CTU14.0-30-ST G02278 CTU14.0-40-ST G02327 CTU14.0-30 G02791 CTU14.0-50-ST G02464 C-CTU14.0-30-ST G02898
- Recall number
- Z-1844-2022
- Recalling firm
- Cook Incorporated
- Product
- Vinyl Connecting Tube, Connecting Tube Reference Part Number/GPN CTU14.0-30-ST G02278 CTU14.0-40-ST G02327 CTU14.0-30 G02791 CTU14.0-50-ST G02464 C-CTU14.0-30-ST G02898
- Status
- Open, Classified
- Initiated
- 2022-08-16
- Posted
- 2022-09-28
- Terminated
- not on file
- Reason
- Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.
- Root cause
- Under Investigation by firm
- Action
- On August 16, 2022, Cook Medical notified affected customers of the recall. Customers were instructed to immediately cease all further distribution and use of the affected products. Affected product should be quarantined and returned to Cook Medical to receive product credit. If you have any questions or concerns, please contact Cook Medical Customer Relations at 800.457.4500 or 812.339.2235
- Quantity
- 240 US; 108 OUS
- Distribution
- Domestic distribution nationwide. Foreign distribution worldwide.
- Lot, serial or model codes
- CTU14.0-30-ST G02278 UDI-DI: 00827002022782 Lots/Expiration Date: 14806993 22-06-2025 14806994 22-06-2025 14806997 22-06-2025 14807003 22-06-2025 14809136 23-06-2025 14809138 23-06-2025 14809140 23-06-2025 14809141 23-06-2025 14811461 24-06-2025 14823426 01-07-2025 14823427 01-07-2025 14823428 01-07-2025 14823429 01-07-2025 14826334 05-07-2025 14826335 05-07-2025 14826337 05-07-2025 14826338 05-07-2025 14831013 07-07-2025 14831014 07-07-2025 14832846 08-07-2025 14833913 08-07-2025 14834825 11-07-2025 14835074 11-07-2025 14835079 11-07-2025 14835400 11-07-2025 14835401 11-07-2025 14836968 12-07-2025 14836973 12-07-2025 14836974 12-07-2025 14836975 12-07-2025 14841346 14-07-2025 14844979 18-07-2025 14844980 18-07-2025 14844981 18-07-2025 14844983 18-07-2025 14844984 18-07-2025 14847734 19-07-2025 14847738 19-07-2025 NS14809137 23-06-2025 NS14832847 08-07-2025 CTU14.0-40-ST G02327 UDI-DI: 00827002023277 Lots/Expiration Date: 14811457 24-06-2025 14811459 24-06-2025 14811460 24-06-2025 14821325 30-06-2025 14821326 30-06-2025 14826333 05-07-2025 14831010 07-07-2025 14832848 08-07-2025 14835078 11-07-2025 14847740 19-07-2025 NS14818298 29-06-2025 CTU14.0-30 G02791 UDI-DI: 00827002027916 Lots/Expiration Dates: 14816266 28-06-2025 14816268 28-06-2025 14816269 28-06-2025 14816273 28-06-2025 14834821 11-07-2025 14835076 11-07-2025 14835077 11-07-2025 14841348 14-07-2025 14841352 14-07-2025 14847735 19-07-2025 NS14816264 28-06-2025 NS14816265 28-06-2025 NS14831012 07-07-2025 NS14851689 21-07-2025 CTU14.0-50-ST G02464 UDI-DI: 00827002024649 Lots/Expiration Date: 14816271 28-06-2025 14831009 07-07-2025 NS14813459 27-06-2025 NS14826331 05-07-2025 NS14826336 05-07-2025 NS14841345 14-07-2025 C-CTU14.0-30-ST G02898 UDI-DI: 00827002028982 Lots/Expiration Date: 14826332 05-07-2025 NS14816270 28-06-2025
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- GCD
- Firm FEI
- 1820334
- Firm city
- Bloomington
- Firm state
- IN
- 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