FDAFDA recall Z-2858-2026 · Aug 12, 2026
Medical Action Industries, Inc. 306: Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Mo recall
Recall found
Product
Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Catalog Number: 78791
Reason for recall
Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- Lot Code: Lot No.: 327075 328690 319980 320965 318461 322375 325653 330775 331356 336680 UDI: 20809160242558
- Quantity
- 3740 kits (180 cases)
- Distribution
- US Nationwide distribution in the state of CA.
- Recalling firm
- Medical Action Industries, Inc. 306, Arden, NC
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-05-21
Source: openFDA enforcement record Z-2858-2026 · search recall number Z-2858-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.