Recalling firm
Medical Action Industries, Inc. 306
Product type
Device
Status
Ongoing
Report date
2026-05-13
Distribution
US distribution to state of: AZ OUS: None
Firm state
NC
Product quantity
2030 kits
Initiated by
Voluntary: Firm initiated
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"
Product description
Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case
Code / lot info
UDI:20809160490294/ Lot numbers: 342509, 346066, 338434, 339423, 337365, 335489, 336189, 336789
Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.