Fresh Recalls

FDAClass I · Medical device · Recall Z-2146-2026 · Recalled May 20, 2026

Medline medical convenience kits recall — Medline Industries, LP

Agency report date: May 20, 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
Medline medical convenience kits
Company / brand
Medline Industries
Lot / serial / date codes
UDI/DI each 10889942814619, UDI/DI case 40889942814610, Lot Number: 26CMC977
Distribution
US (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK.
Agency product description and boundaries

Medline medical convenience kits, containing Namic Manifold, Labeled as: HEART CATH PACK-LF, Medline Kit Number/SKU DYNJ36478B

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: Medline has identified the presence of particulate within the fluid path of the Manifolds.

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

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: Medline medical convenience kits

3. Open the official notice or contact

Official recall ID
Z-2146-2026
Brand
Medline Industries
Classification
Class I
Units affected
0 kits
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Northfield, IL, United States
Firm address
3 Lakes Dr, 60093-2753

Identifying details (verbatim from the notice)

Product codes / lots
UDI/DI each 10889942814619, UDI/DI case 40889942814610, Lot Number: 26CMC977
Distribution
US (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK.
Firm notified the public via
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA event ID
98735
Recall initiated
March 24, 2026
FDA classified
May 8, 2026
FDA report date
May 20, 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 August 18, 2026 at 6:00 PM UTC.

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