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.