The FDA has posted 5 enforcement recalls from Medical Action Industries, Inc. 306 since 2025, including 4 Class I (most serious) recalls. Most recent report: Sep 16, 2026.
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.
Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be introduced into blood circulation and become lodged within bl…
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"
Firm name as filed with the FDA: “Medical Action Industries, Inc. 306”. Related firm entities may file under separate names. Source: U.S. FDA openFDA device enforcement reports. Informational only — verify with the FDA before acting.