Fresh Recalls

FDAClass II · Medical device · Recall Z-2858-2026 · Recalled August 12, 2026

Brand Name recall — Medical Action Industries, Inc. 306

Agency report date: August 12, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Brand Name
Company / brand
Medical Action Industries
Lot / serial / date codes
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.
Agency product description and boundaries

Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Catalog Number: 78791

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Brand Name

3. Open the official notice or contact

Official recall ID
Z-2858-2026
Brand
Medical Action Industries
Classification
Class II
Units affected
3740 kits (180 cases)
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Arden, NC, United States
Firm address
25 Heywood Rd, 28704-9302

Identifying details (verbatim from the notice)

Product codes / lots
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.
Firm notified the public via
E-Mail
FDA event ID
99338
Recall initiated
May 21, 2026
FDA classified
August 3, 2026
FDA report date
August 12, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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