- Recalling firm
- Medline Industries, LP
- Reason for 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.
- Affected products (lot / model / serial)
- DYNJ48258D UDI-DI 10889942563272 Lots 23CBH459 23GBJ128 24ABM400
- Units affected
- 90 kits (US)
- Distribution pattern
- US Nationwide distribution in the states of MN and SD.
- Firm location
- Northfield, IL, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-3229-2026
- Recall initiated
- August 10, 2026
- FDA classification date
- September 18, 2026
- FDA report date
- September 30, 2026
- FDA event ID
- 99729
- Last updated on HTM Vibe
- October 6, 2026
