FDA Medical Device Recalls (openFDA)
Medline Industries, LP: ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC
- Recall number
- Z-1690-2026
- Recalling firm
- Medline Industries, LP
- Product
- ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC
- Status
- Open, Classified
- Initiated
- 2026-02-13
- Posted
- 2026-03-27
- Terminated
- not on file
- Reason
- Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage. Leakage may result in delayed care and fluid loss. Additional consequences may also occur if user over-tightens the connector to stop the leakage, including additional clinical intervention, risk of infection, patient discomfort, and prolonged recovery process.
- Root cause
- Process change control
- Action
- On February 13, 2026, the firm notified affected consignees via Urgent Medical Device Recall letters delivered through First Class mail and email. Customers were instructed to destroy all affected ENFit G-Tube connectors and kits that contain the G-Tube connectors.
- Quantity
- 651,789
- Distribution
- Worldwide - US Nationwide and the countries of Canada.
- Lot, serial or model codes
- UDI-DI 10888277314719 (ea) 40888277314710(case) All Lots
- 510(k) numbers
- ["K151628"]
- PMA numbers
- not on file
- Product code
- PIO
- Firm FEI
- 1417592
- Firm city
- Northfield
- Firm state
- IL
- 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