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FDA recall, , Moderate risk

Medical Action Industries Dialysis Change Tray Clear Sequence

The Dialysis Change Tray Clear Sequence has an improper seal that may cause doming or tearing of the silicone seal.

What happened

Medical Action Industries, Inc., located in Arden, North Carolina, recalled its Dialysis Change Tray Clear Sequence because the convenience kits contain a needle free access device that has an improper seal, which may result in doming or tearing of the silicone seal. The recall began on May 21, 2026, and was added to the FDA's Enforcement Report on August 3, 2026.

The product was distributed in California. The recall involved 3740 kits (180 cases).

What to do

We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:

  1. A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
  2. Talk to your health care provider before you stop using it.

Is yours affected?

Match the model number and lot code listed under your product.

  1. Dialysis Change Tray Clear Sequence

    Model number
    • 78791
    Lot code
    • 327075
    • 328690
    • 319980
    • 320965
    • 318461
    • 322375
    • 325653
    • 330775
    • 331356
    • 336680

Recall details

Company began the recall
Sold in

US Nationwide distribution in the state of California.

Company
Medical Action Industries, Inc. 306Arden, North Carolina
Risk

Moderate risk

Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.

FDA Class II recall · How risk is rated

Event ID
99338
Recall number
Z-2858-2026
Quantity recalled
3740 kits (180 cases)

All recalls from Medical Action Industries, Inc. 306

Timeline

FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.

  1. Company began the recall

  2. Added to FDA's Enforcement Report · Classified by FDA

  3. Listed on Recall Canary

  4. In FDA's weekly enforcement report

  5. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 2, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)