FDA Medical devices recall ·
Medical Action Industries Product Name: Dialysis Change Tray Clear… recall
- Recall number
- Z-2858-2026
- Date
- (initiated May 21, 2026)
- Company / brand
- Medical Action Industries, Inc. 306
25 Heywood Rd, Arden, NC, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 3740 kits (180 cases)
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Catalog Number: 78791
Why was it recalled?
Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot Code: Lot No.: 327075 328690 319980 320965 318461 322375 325653 330775 331356 336680 UDI: 20809160242558
Distribution
US Nationwide distribution in the state of CA.
States: California
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2858-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.