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:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- 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.
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
- Hazard
- Device defect
- 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.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated



