FDA recall Z-2007-2026

Product

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

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

Key facts

Status

Ongoing

Initiation date

2026-03-17

Report date

2026-05-13

Voluntary/Mandated

Voluntary: Firm initiated

Location

Arden, NC, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2007-2026