FDA recall record

Medical Action Industries Inc recall — FDA Z-2007-2026

Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between…

Class Iclassification
Z-2007-2026official record ID
May 13, 2026report date

Recall record at a glance

Official recordZ-2007-2026
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmMedical Action Industries, Inc. 306
Report dateMay 13, 2026
Recall initiation dateMar 17, 2026
Quantity2030 kits
LocationArden, NC, United States

Official product description

Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case

Why the product was recalled

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"

Distribution information

US distribution to state of: AZ OUS: None

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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