Medline Convenience Kits Containing Healthmark Instrument Channel Brushes
Medline convenience kits contain brushes with a sharp edge that can cut and infect.
Moderate risk
Using it may cause temporary or medically reversible health problems. Serious harm is unlikely.
FDA Class II recall · How risk is rated
2 photos
What happened
Medline Industries, LP, of Northfield, Illinois, began a recall on August 10, 2026, of Medline convenience kits containing Healthmark Instrument Channel Brushes. The kits are SINUS PACK DYNJ48258D and Sinus Pack DYNJ48258F. The brushes were recalled by the manufacturer due to the potential for a sharp edge/burr on the end of the brush, which can cause cut injury/abrasion and infection.
The recall involves 90 kits distributed in Minnesota and South Dakota. The FDA added the recall to its Enforcement Report on September 18, 2026.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is your kit affected?
Compare the details below with your product and check the FDA notice to confirm whether it is affected.
Medline convenience kits containing Healthmark Instrument Channel Brushes. Sinus Pack DYNJ48258D and Sinus Pack DYNJ48258F.
- UDI-DI
- 10889942563272
- Lot
- 24HBR684
- 25CBS234
- 25GBH438
- 25JBC863
- 26FBU052
- UDI-DI
- 10198459038334
Some entries omit identifying details. Check the notice to confirm which units are affected.
Details
- Company began the recall
- Sold in
US Nationwide distribution in the states of Minnesota and South Dakota.
- Event ID
- 99729
- Recall numbers
- Z-3229-2026 to Z-3230-2026
- Company
- Medline Industries, LPNorthfield, Illinois
- Hazard
- Device defect
- Quantity recalled
- 90 kits (US)
- Recall type
- Voluntary: Firm initiated
- Customers told by
- Letter
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
