FDA-Device2026-05-20Class IPROCESSING DEFECT
Medline Namic Preceptor blood pressure manifold recalled for particulate contamination
OTHERNationwide distribution
Medline Namic Preceptor manifold recalled for particulate contamination
Medline has identified particles inside the fluid path of certain Namic Preceptor Manifold blood pressure transducers. These particles could interfere with accurate blood pressure readings or damage the device during use.
- Check if your device matches one of the affected lot numbers listed in the recall notice.
- Contact Medline or your healthcare facility immediately if you have an affected unit.
- Do not use the device until you have confirmed it is not affected or have received a replacement.
Hazard
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Sold states
US (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK.
Affected count
6390 units
Manufactured in
3 Lakes Dr, Northfield, IL, United States
Products
Namic Preceptor Manifold, custom, Medline Product Number/SKU 64037107; Extravascular blood pressure transducer
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2141-2026More Medline Industries, LP recalls
- FDA-Device2026-05-20Medline TAVI medical convenience kits recalled for particulate contamination in fluid path
- FDA-Device2026-05-20Medline medical convenience kits with Namic Manifold recalled for particulate contamination
- FDA-Device2026-05-20Medline cardiac catheterization manifold kits recalled for particulate contamination
- FDA-Device2026-05-20Medline Namic Angiographic Manifold recalled for particulate contamination in fluid path
- FDA-Device2026-05-20Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038200; Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.
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