CLASS I ONGOING Device recall · Reported 20 May 2026 · FDA Enforcement Report
Namic Preceptor Manifold, custom, Medline Product Number recalled
Medline Industries is recalling Namic Preceptor Manifold, custom, Medline Product Number, distributed nationwide in the US. The recall was initiated on 24 Mar 2026 and the FDA has classified it as Class I.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2142-2026
- FDA event ID
- 98735
- Recalling firm
- Medline Industries, Northfield, IL
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 24 Mar 2026
- FDA classified
- 8 May 2026
- Reported
- 20 May 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Particulate Matter
- Device type
- Heart & Vascular Devices
Timeline
| 24 Mar 2026 | Recall initiated by company | |
| 8 May 2026 | Classified by FDA | +45 days |
| 20 May 2026 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Product as listed by the FDA
Namic Preceptor Manifold, custom, Medline Product Number/SKU 64039307; Extravascular blood pressure transducer
Where it was distributed
US (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK.
Questions about this recall
Why was it recalled?
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Which lots are affected?
UDI/DI each 10193489059205, UDI/DI case 30193489059209, Lot Numbers: 117277, 119982, 122210, 122199, 130129, 133014, 136396, 138613, 139138, 157974, 162399, 164317, 175538, 193515, 193531.
Where was it sold?
US (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
8 other products · FDA event 98735This product is part of a recall event; the main page for the event is Medline medical convenience kits, containing Namic Manifold recalled.
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