Medline Industries, LP recalls Namic Angiographic Manifold
- Recalling company
- Medline Industries, LP
- Product
- Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038200; Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.
- Reason
- Medline has identified the presence of particulate within the fluid path of the Manifolds.
- Classification
- Class I – a reasonable probability that use will cause serious adverse health consequences or death
- Recall date
- Mar 24, 2026
- Reported
- May 20, 2026
- Distribution
- US (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK.
- Status
- Ongoing
- Quantity
- 7075 units
- Lot / codes
- UDI/DI each 10193489059144, UDI/Di case 30193489059148, Lot Numbers: 90184, 94779, 97786, 106351, 108597, 109876, 114056, 114989, 115459, 115931, 116358, 116865, 118245, 122974, 126077, 127795, 129531, 130557, 136114, 150501, 151591, 152772, 154514, 156045, 160318, 163255, 168053.
- Company location
- Northfield, IL
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2138-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2138-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.