Medline NAMIC RA Control Syringe Kit Recall
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follo
Updated February 27, 2026
Medline has recalled three medical convenience kits containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes. The rotating adaptor on the syringe can unwind during use, causing a loose or complete disconnection between the syringe and manifold, a serious risk during medical procedures.
Is the Medline Industries, LP recalled? Yes. This product was recalled by FDA on February 27, 2026. Details below.
What is recalled
Medline medical convenience kits containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), sold under three SKUs: 1. NON VASCULAR PACK, Medline SKU # DYNJ68037C 2. VEIN, Medline SKU # DYNJ89845 3. VEIN, Medline SKU # DYNJ89845A
Am I affected
You are affected if your facility has Medline medical convenience kits with any of the following SKUs printed on the label: DYNJ68037C, DYNJ89845, or DYNJ89845A. Check the product packaging for these Medline SKU numbers.
What to do right now
Stop using these kits immediately and quarantine any remaining inventory. This recall was initiated by Medline Industries, LP. Because no consumer contact information was provided in the recall record, contact Medline Industries, LP directly or visit the FDA recall page at https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts for the latest guidance and remedy instructions.
The hazard
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Brands affected
- Source
- FDA
- Category
- Medical Devices
- Recall ID
- fda-Z-1719-2026
- Classification
- Class I
- Recalled
- February 27, 2026
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