Recall Z-2465-2021— CAREFUSION

Name: FDA recall Z-2465-2021
Creator: U.S. Food and Drug Administration
Published: 2021-08-02

Class II · Ongoing

Class II FDA medical device recall by CAREFUSION, initiated 2021-08-02. It names one FDA 510(k) clearance: K931550. Product: BD SE Burette Set 20 Drops 2 Injection Ports Vented/NonVented, REF: 72103E-0006. Reason: Needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial or total occlusions, which could lead to therapy delay. Follow-up activates not required if product has already been used or was safely connected to the female luer of connecting device..

Recalling firm: CAREFUSION
Classification: Class II
Status: Ongoing
Initiated: 2021-08-02
Firm location: San Diego, CA, United States

510(k) clearances named in this recall

1 on FDA's record

K931550 — EZ ADMINISTRATION SETY·cleared 1994-01-10

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

BD SE Burette Set 20 Drops 2 Injection Ports Vented/NonVented, REF: 72103E-0006

Reason for recall

Needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial or total occlusions, which could lead to therapy delay. Follow-up activates not required if product has already been used or was safely connected to the female luer of connecting device.

Data sourced from openFDA. This site is unofficial and independent of the FDA.