Medical Action Industries, Inc. 306

Medical Action Industries, Inc. 306: 6 recalls listed since May 2026 across FDA; 3 rated high risk.

By year

An internal data-entry error caused kit lot 333606 to be labeled with an expiration date of March 31, 2027, instead of February 28, 2027.

Low riskFDAOct 2, 2026Labeling error

Medical Action Blood Culture Collection Kits contain applicators with an open or incomplete seal that may compromise sterility and lead to infection.

Moderate riskFDASep 16, 2026Sterility problem

Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.

High riskFDASep 9, 2026Sterility problem

The Dialysis Change Tray Clear Sequence has an improper seal that may cause doming or tearing of the silicone seal.

Moderate riskFDAAug 3, 2026Device defect

Cardiovascular procedure kits contain manifolds that may have particulate within the fluid path, which could become lodged in blood vessels.

High riskFDAJul 30, 2026Foreign object

Pack Cath BHH contains a syringe whose rotating adapter may unwind, causing loose or full disconnection.

High riskFDAMay 6, 2026Device defect