FDA Medical devices recall ·
Medline convenience kits containing Healthmark Instrument Channel Brushes recall
- Recall number
- Z-3229-2026
- Date
- (initiated August 10, 2026)
- Company / brand
- Medline Industries, LP
3 Lakes Dr, Northfield, IL, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 90 kits (US)
- Hazard tags
- Laceration Injury risk
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and Sinus Pack DYNJ48258F.
Why was it recalled?
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 should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
DYNJ48258D UDI-DI 10889942563272 Lots 23CBH459 23GBJ128 24ABM400
Distribution
US Nationwide distribution in the states of MN and SD.
States: Minnesota South Dakota
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-3229-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.