- Recalling firm
- Medline Industries, LP
- Reason for recall
- Medline has identified the presence of particulate within the fluid path of the Manifolds.
- Affected products (lot / model / serial)
- UDI/DI each 10193489059182, UDI/DI case 30193489059186, Lot Numbers: 92261, 152082, 163966, 163256.
- Units affected
- 1975 units
- Distribution pattern
- US (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK.
- Firm location
- Northfield, IL, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2140-2026
- Recall initiated
- March 24, 2026
- FDA classification date
- May 8, 2026
- FDA report date
- May 20, 2026
- FDA event ID
- 98735
- Last updated on HTM Vibe
- July 24, 2026