Medical Action Industries, Inc. 306 Recalls

6 recalls on record in the United States

medical: 6
medical Class I
2026-05-13

Medical Action Industries, Inc. 306 recalls Medical Action Industries Inc. Pack Cath BHH, REF: BHCA4

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"

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medical Class I
2026-08-05

Medical Action Industries, Inc. 306 recalls Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing

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 blood vessels.

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medical Class II
2026-08-12

Medical Action Industries, Inc. 306 recalls Brand Name: Medical Action Industries Product Name: Dialys

Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.

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medical Class I
2026-09-16

Medical Action Industries, Inc. 306 recalls Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Sh

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

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medical Class I
2026-09-16

Medical Action Industries, Inc. 306 recalls Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium C

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

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medical Class II
2026-09-23

Medical Action Industries, Inc. 306 recalls Blood Culture Collection Venipuncture Kit 20/Cs, REF: 77451;

Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may compromise the component's sterile barrier and if used may lead to localized skin or soft tissue infection.

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