- 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 10193489059137, UDI/DI case 30193489059131, Lot Numbers: 89181, 95326, 95254, 102287, 102286, 102706, 105362, 105558, 108608, 112242, 112243, 115437, 118477, 121180, 121645, 122708, 126024, 131603, 136583, 140860, 142371, 146728, 147474, 148571, 152020, 153175, 163216, 175580, 176810, 184394, 191388, 193141.
- Units affected
- 6390 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-2141-2026
- 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