Product Wiki · Recalls · U.S. FDA — Device Enforcement

Convenience Kits from Centurion that contain an In-Vision- Plus Needleless IV Connector, Model: code RYM5001 InVision-Plus¿ Needless IV Connectors are used for single patient use in IV and blood administration sets without the need for needles, thus eliminating the potential for needle-stick inj — recall Z-0861-2016

U.S. FDA — Device Enforcement · United States · 2016-01-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0861-2016
Date of alert
2016-01-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Centurion Medical Products Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
2015042150
Reported risk: Convenience Kits contain an In-Vision-Plus Needleless IV Connector, code RYM5001 that is being recalled by the manufacturer, RyMed Technologies, LLC. A component molding abnormality may cause female luer threads to crack, leading to potential for the mating tubing set to become detached and for the administration to be interrupted. Other components within these kits are not affected.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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