FDAOctober 8, 2019device

Arrow EZ-IO Intraosseous Vascular Access System 45mm Needle+Stabilizer Kit, Product Code 9079P-VC-005 - Product Usage: The Arrow EZ-IO Intraosseous Vascular Access System provides intraosseous access in the proximal humerus, proximal tibia, and distal tibia of adult and pediatric patients, and th...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The safety cap attached to needles within the needle sets may become dislodged exposing the needle and potentially causing the needle to protrude through the packaging. If this issue is not detected, the immediate risk of exposure to the affected devices is needle stick injury to the clinician or health care professional. In addition, a puncture of the packaging may compromise the sterility of the needle.

What to do

FDA enforcement status: Ongoing

Brands named

teleflex medicalteleflex

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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