Fresh Recalls

FDAClass II · Medical device · Recall Z-3230-2026 · Recalled September 30, 2026

Medline convenience kits containing Healthmark Instrument Channel Brushes recall — Medline Industries, LP

Agency report date: September 30, 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 convenience kits containing Healthmark Instrument Channel Brushes
Company / brand
Medline Industries
Lot / serial / date codes
DYNJ48258F UDI-DI 10198459038334 Lots 24HBR684 25CBS234 25GBH438 25JBC863 26FBU052
Distribution
US Nationwide distribution in the states of MN and SD.
Agency product description and boundaries

Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and SINUS PACK DYNJ48258F.

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: Kits contain Healthmark Instrument Channel Brushes, which were recalled by the manufacturer due to the potential for a sharp edge/burr on the end of the brush. Potential hazards associated include cut injury/abrasion and infection.

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: Medline convenience kits containing Healthmark Instrument Channel Brushes recall status

3. Open the official notice or contact

Official recall ID
Z-3230-2026
Brand
All Medline Industries recalls
Classification
Class II
Units affected
90 kits (US)
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
DYNJ48258F UDI-DI 10198459038334 Lots 24HBR684 25CBS234 25GBH438 25JBC863 26FBU052
Distribution
US Nationwide distribution in the states of MN and SD.
Firm notified the public via
Letter
FDA event ID
99729
Recall initiated
August 10, 2026
FDA classified
September 18, 2026
FDA report date
September 30, 2026

More Medline Industries recalls

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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 October 22, 2026 at 6:00 PM UTC. Record retrieved October 22, 2026 at 6:00 PM UTC.

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