Fresh Recalls

Medical Action Industries recalls

7 recent recalls on record for Medical Action Industries in connected official government data as of October 22, 2026 at 12:00 PM UTC.

Models with recalls

Blood Culture Collection Venipuncture Kit 20/Cs (1)Brand Name (1)Generic Name (1)Kit (2)Medical Action Industries Inc (1)Pack Angiography NCMC 3/Cs BANNER (1)

All Medical Action Industries recalls

FDA Class III · Medical device · October 14, 2026

Generic Name recall — Medical Action Industries, Inc. 306

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.

Official ID Z-0069-2027 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Blood Culture Collection Venipuncture Kit 20/Cs recall — Medical Action Industries, Inc. 306

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 componen…

Official ID Z-3181-2026 · Official record ↗

FDA Class I · Medical device · September 16, 2026

Kit recall — Medical Action Industries, Inc. 306

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

Official ID Z-3107-2026 · Official record ↗

FDA Class I · Medical device · September 16, 2026

Kit recall — Medical Action Industries, Inc. 306

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

Official ID Z-3106-2026 · Official record ↗

FDA Class II · Medical device · August 12, 2026

Brand Name recall — Medical Action Industries, Inc. 306

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

Official ID Z-2858-2026 · Official record ↗

FDA Class I · Medical device · August 5, 2026

Pack Angiography NCMC 3/Cs BANNER recall — Medical Action Industries, Inc. 306

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…

Official ID Z-2792-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

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

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"

Official ID Z-2007-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 12:00 PM UTC.