FDAClass I · Medical device · Recalled May 13, 2026

Medical Action Industries Inc recall — Medical Action Industries, Inc. 306

Hazard: 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: most serious — reasonable probability of serious health consequences or death.

View the official FDA enforcement record (openFDA) ↗

Official recall ID: Z-2007-2026
Brand: Medical Action Industries
Classification: Class I
Units affected: 2030 kits
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Description

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

Affected products

Medical Action Industries Inc

Companies & origin

Recalling firm location: Arden, NC, United States
Firm address: 25 Heywood Rd, 28704-9302

Identifying details (verbatim from the notice)

Product codes / lots: UDI:20809160490294/ Lot numbers: 342509, 346066, 338434, 339423, 337365, 335489, 336189, 336789
Distribution: US distribution to state of: AZ OUS: None
Firm notified the public via: Letter
FDA event ID: 98698
Recall initiated: March 17, 2026
FDA classified: May 6, 2026
FDA report date: May 13, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 24, 2026 at 3:00 AM UTC.

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