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Class IIOngoing

Medline Industries, LP recalls 2 products

Recall date · record updated Sep 30, 2026 · Source: U.S. Food and Drug Administration (openFDA device enforcement)

What to do

Check your product against the names and codes above. The FDA enforcement record lists the recall as voluntary: firm initiated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.

Company
Medline Industries, LP
Reason
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.
Hazard
FDA Class II: may cause temporary or medically reversible adverse health consequences (FDA definition).
Who’s affected
US Nationwide distribution in the states of MN and SD.
Where
Nationwide
Official notice
www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99729…

Products (2)

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

    Codes/lots: DYNJ48258D UDI-DI 10889942563272 Lots 23CBH459 23GBJ128 24ABM400Quantity: 90 kits (US)Recall no. Z-3229-2026Class II

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

    Codes/lots: DYNJ48258F UDI-DI 10198459038334 Lots 24HBR684 25CBS234 25GBH438 25JBC863 26FBU052Quantity: 90 kits (US)Recall no. Z-3230-2026Class II

Update history

  1. First listed on OVERLOOKED from the official record.

When the agency expands or changes this recall, we update this page and log the change here.

Proof: raw official record (JSON) · fetched from FDA API

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