FDA-Device2026-05-20Class IPROCESSING DEFECT
Medline Namic Preceptor blood pressure manifold recalled for particulate contamination
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.
Who it affects
Adults
Illnesses reported
None reported
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 recalls
- FDA-PR2026-08-05Medline Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits recalled for connector overheating risk
- FDA-Device2026-07-29Medline surgical convenience kits recalled for quality issues in anesthetic component
- FDA-Device2026-07-29Medline NEURO PACK medical kits recalled for Bacillus contamination
- FDA-Device2026-07-29Medline convenience kits with Bard Silastic Foley Catheters recalled for surface contamination
- FDA-Device2026-07-29Medline convenience kits with Bard Silastic Foley Catheters recalled for surface contamination
Don't want to check this manually?
We email you a Sunday digest of new federal recalls relevant to your household — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.
Get the Sunday Brief