Namic Preceptor Manifold recall: Particulate Matter
Namic Preceptor Manifold, custom, Medline Product Number/SKU 64037107; Extravascular blood pressure transducer
Why was Namic Preceptor Manifold recalled?
Medline has identified the presence of particulate within the fluid path of the Manifolds.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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.
- Product
- Namic Preceptor Manifold, custom, Medline Product Number/SKU 64037107; Extravascular blood pressure transducer
- Recalling firm
- Medline Industries, LP
- Quantity
- 6390 units
- Distribution
- US (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK.
- Recall date
- May 20, 2026
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)