FDA recall record

Medical Action Industries Dialysis Change Tray Clear Sequence recall — FDA Z-2858-2026

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

Class IIclassification
Z-2858-2026official record ID
Aug 12, 2026report date

Recall record at a glance

Official recordZ-2858-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmMedical Action Industries, Inc. 306
Report dateAug 12, 2026
Recall initiation dateMay 21, 2026
Quantity3740 kits (180 cases)
LocationArden, NC, United States

Official product description

Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Catalog Number: 78791

Why the product was recalled

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

Distribution information

US Nationwide distribution in the state of CA.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

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.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.

Medical DeviceMay 13, 2026

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 the syringe and manifold"

Class IFDA: OngoingMedical Action Industries, Inc. 306