FDAClass I · Medical device · Recalled May 20, 2026
Namic Preceptor Manifold recall — Medline Industries, LP
Hazard: Medline has identified the presence of particulate within the fluid path of the Manifolds.
Class I: most serious — reasonable probability of serious health consequences or death.
View the official FDA enforcement record (openFDA) ↗
- Official recall ID
- Z-2141-2026
- Brand
- Medline Industries
- Classification
- Class I
- Units affected
- 6390 units
- Recall status
- Ongoing
- Initiated
- Voluntary: Firm initiated
Description
Namic Preceptor Manifold, custom, Medline Product Number/SKU 64037107; Extravascular blood pressure transducer
Affected products
Companies & origin
- Recalling firm location
- Northfield, IL, United States
- Firm address
- 3 Lakes Dr, 60093-2753
Identifying details (verbatim from the notice)
- Product codes / lots
- 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.
- Distribution
- US (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK.
- Firm notified the public via
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- FDA event ID
- 98735
- Recall initiated
- March 24, 2026
- FDA classified
- May 8, 2026
- FDA report date
- May 20, 2026
Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim;
the linked government source is authoritative. Source last checked July 24, 2026 at 3:00 AM UTC.
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