Medline NAMIC Angiographic Syringe Recall
NAMIC Angiographic Control Syringe, labeled as follows: 1. SYRINGE,7ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70083007; 2. SYRINGE,8ML,TR/FR,RA,W
Updated February 27, 2026
Medline Industries is recalling several sizes of NAMIC Angiographic Control Syringes because the rotating adaptor may unwind during use, causing the syringe to loosen or fully disconnect from the manifold. A disconnection during an angiographic procedure could interrupt treatment and pose a serious risk to patients.
Is the Medline Industries, LP recalled? Yes. This product was recalled by FDA on February 27, 2026. Details below.
What is recalled
NAMIC Angiographic Control Syringes distributed by Medline Industries, LP, in the following six configurations: 1. 7 mL syringe with reservoir, Medline SKU 70083007 2. 8 mL syringe with reservoir, Medline SKU 70084007 3. 8 mL syringe without reservoir (MTS), Medline SKU 70084017 4. 7 mL syringe with reservoir (OEM), Medline SKU 80083007 5. 8 mL syringe with reservoir (OEM), Medline SKU 80084007 6. 8 mL syringe without reservoir (MTO/OEM), Medline SKU 80084017
Am I affected
You are affected if your facility is using NAMIC Angiographic Control Syringes supplied by Medline Industries with any of these SKUs: 70083007, 70084007, 70084017, 80083007, 80084007, or 80084017. Check the product packaging or inventory records for these Medline SKU numbers.
What to do right now
Stop using any affected syringes immediately and quarantine remaining stock. Because no consumer contact information was provided in the recall notice, 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-1713-2026
- Classification
- Class I
- Recalled
- February 27, 2026
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