Medline Industries, LP recalls Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and Sinus Pack
Medline recalls specific sinus packs containing Healthmark Instrument Channel Brushes with potential sharp edges that could cause cuts or infection. Affected units include SINUS PACK DYNJ48258D and DYNJ48258F models.
Lower-risk recall
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.
What happened, in plain English
Medline is recalling convenience kits with Healthmark Instrument Channel Brushes due to a possible sharp edge or burr on the brush that could cause cuts or infection. This affects specific sinus packs sold with model numbers DYNJ48258D and DYNJ48258F. Read more at govinfonow.com/recall/1292620-medline-sinus-packs-with-sharp-brush-edges-recalled-for-cut.
Source Summary by GovInfoNow · govinfonow.com/recall/1292620-medline-sinus-packs-with-sharp-brush-edges-recalled-for-cut · Published October 6, 2026 · Updated October 6, 2026 · FDA enforcement record: FDA #Z-3229-2026
Cite this page
“Medline Sinus Packs with Sharp Brush Edges Recalled for Cut Risk.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/1292620-medline-sinus-packs-with-sharp-brush-edges-recalled-for-cut. Based on FDA recall #Z-3229-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3229-2026%22&limit=1).
Why it’s dangerous
The Healthmark Instrument Channel Brushes in these kits may have a sharp edge or burr that can cause cuts or infection if the brush is used improperly. This is a minor hazard that does not pose a high risk of serious injury.
Who’s affected
Healthcare professionals using these kits for sinus procedures are most at risk. The recall applies to specific models sold in the U.S. between 2023 and 2024.
How to tell if you have this one
Check for model numbers DYNJ48258D or DYNJ48258F on the packaging. These kits were sold with lot numbers 23CBH459, 23GBJ128, and 24ABM400 between 2023 and 2024.
- Brand
Medline- Category
Medical device
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Ongoing- Distribution
US Nationwide distribution in the states of MN and SD.
| Recall number | Product, codes & lots |
|---|---|
| Z-3229-2026 | Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and Sinus Pack DYNJ48258F.; DYNJ48258D UDI-DI 10889942563272 Lots 23CBH459 23GBJ128 24ABM400 |
| Z-3230-2026 | Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and SINUS PACK DYNJ48258F.; DYNJ48258F UDI-DI 10198459038334 Lots 24HBR684 25CBS234 25GBH438 25JBC863 26FBU052 |
What to do — step by step
Check Product Model
Look for model numbers DYNJ48258D or DYNJ48258F on the packaging.
Questions people ask
What is the hazard with these kits?
The Healthmark Instrument Channel Brushes may have a sharp edge or burr that could cause cuts or infection.
How can I tell if I have the recalled product?
Check for model numbers DYNJ48258D or DYNJ48258F on the packaging. These kits were sold with lot numbers 23CBH459, 23GBJ128, and 24ABM400 between 2023 and 2024.
What should I do if I have the recalled product?
The recall does not specify a remedy, so contact Medline directly for guidance.
Contact Medline
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3229-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-3229-2026 from Medline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Similar recalls
Keep exploring
From people who’ve dealt with this
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-3229-2026 (August 10, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3229-2026 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.