Class I

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

Medical Action Industries, Inc. 306 · March 17, 2026

Reason for Recall

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"

Distribution

US distribution to state of: AZ OUS: None

States Affected

AZ

Quantity Affected

2030 kits

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2007-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

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