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Lower risk Medical device recall · FDA · Published May 21, 2026

Medical Action Industries Dialysis Change Tray Clear Sequence: Silicone Seal Risk

Recall of Medical Action Industries Dialysis Change Tray Clear Sequence model 78791 due to improper silicone seal that may cause doming or tearing. Affected units sold with specific lot codes.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2858-2026Medical deviceMedical Action Industries ›
✎ GovInfoNow plain-language explainer

Medical Action Industries is recalling its Dialysis Change Tray Clear Sequence model 78791 because the silicone seal may dome or tear, potentially causing leaks during dialysis. This could lead to complications for patients using the device. Read more at govinfonow.com/recall/314510-medical-action-industries-dialysis-change-tray-clear-sequence-silicone-seal.

Source Summary by GovInfoNow · govinfonow.com/recall/314510-medical-action-industries-dialysis-change-tray-clear-sequence-silicone-seal · Updated August 18, 2026 · FDA enforcement record: FDA #Z-2858-2026

Cite this page

“Medical Action Industries Dialysis Change Tray Clear Sequence: Silicone Seal Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/314510-medical-action-industries-dialysis-change-tray-clear-sequence-silicone-seal. Based on FDA recall #Z-2858-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2858-2026%22&limit=1).

The FDA announced on May 21, 2026, that Medical Action Industries is recalling its Dialysis Change Tray Clear Sequence kits due to improper seals in the needle-free access device. The agency stated the hazard may result in doming or tearing of the silicone seal.

How to tell if you have it

  • Brand: Medical Action Industries
  • Product Name: Dialysis Change Tray Clear Sequence
  • Model/Catalog Number: 78791
  • Lot Codes: 327075, 328690, 319980, 320965, 318461, 322375, 325653, 330775, 331356, 336680
  • UDI: 20809160242558

The hazard

The convenience kits contain a needle-free access device with an improper seal that may result in doming or tearing of the silicone seal, according to the FDA.

Context

GovInfoNow's records show Medical Action Industries has 14 other recalls on record since December 2, 2019. Other recent recalls include Blood Culture Kits Risk Localized Infection Due to Packaging Seal (July 23, 2026), Epidural Pain Kit Recall: Potentially Compromised Sterility Risk (July 23, 2026), and Pack Angiography Kits Risk Blood Clots from Particulate (May 13, 2026). Similar recent recalls of dialysis products include Medline Dialysis Dressing Kits Recall: Silicone Seal Issues May Cause Blood Flow Problems (Jan. 8, 2026), Medline Dialysis Kits Recall: Silicone Seal Issues May Cause Blood Flow Problems (Jan. 8, 2026), and Medline Dialysis Kits Recall: Silicone Seal Issues May Cause Blood Product Leakage (Jan. 8, 2026).

How to tell if you have this one

Check for the model number 78791 on the tray. Affected units have specific lot codes: 327075, 328690, 319980, 320965, 318461, 322375, 325653, 330775, 331356, 336680.

  • Brand
    Medical Action Industries
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check for Recalled Model

    Look for model number 78791 on the Dialysis Change Tray Clear Sequence.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “US Nationwide distribution in the state of CA.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 3 months after the firm started it.

1. Firm started the recall: May 21, 202612. FDA classified it Class II: Aug 3, 202623. Published in FDA’s Enforcement Report: Aug 12, 202634. Added to GovInfoNow: Aug 18, 202642026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-2858-2026 (May 21, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2858-2026 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA