Critical Alert
Medical Action Industries Recalls Medical Action Industries Inc
This is a Class I recall — the most serious type. There is a reasonable probability of serious health consequences or death.
Source: FDA
CriticalRecall #Z-2007-2026Medical Device
Medical Action Industries Recalls Medical Action Industries Inc
Medical Action Industries, Inc. 306 · Class I — Most Serious
Product Description
Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case
Reason for Recall
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"
FDA Classification
Class I — Most Serious
A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Distribution
US distribution to state of: AZ OUS: None
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
Medical Action Industries, Inc. 306 is recalling a medical device classified as Class I by the FDA — the highest risk level. The recall was initiated on March 17, 2026 affecting 2030 kits. 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". It was distributed nationwide. Consumers and healthcare professionals should exercise caution and discontinue use of the recalled product. Contact the recalling firm directly for return or disposal instructions.
Sources: FDA openFDA Enforcement Database
This recall appears in: Medical Device Defects.