Medical device recalls High risk

Medical Action Industries, Inc. 306 recalls Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case

Recall date
March 17, 2026
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2007-2026
FDA classification
Class I
Brand / firm
Medical Action Industries, Inc. 306
Sold / distributed
US distribution to state of: AZ OUS: None

Why it was recalled

Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case

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