- Recalling firm
- Medline Industries, LP
- Reason for recall
- Unapproved design changes to the products outside of the 510(k) clearance.
- Affected products (lot / model / serial)
- DYNJ0373061J UDI-DI 10889942396856 (EA) 40889942396857 (CS) LOT 24ABR895
- Units affected
- 270,311 total
- Distribution pattern
- Worldwide distribution - US Nationwide and the countries of Canada, Panama, Barbados.
- 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-1889-2026
- Recall initiated
- February 27, 2026
- FDA classification date
- April 17, 2026
- FDA report date
- April 29, 2026
- FDA event ID
- 98601
- Last updated on HTM Vibe
- July 24, 2026