Reported Apr 15, 2026 · Ongoing
NAMIC Angiographic Control Syringe, labeled as follows
Medline Industries, LP
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medline Industries, LP · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
NAMIC Angiographic Control Syringe, labeled as follows
6 of 6 products
| Model / number | Product as published |
|---|---|
70083007 | SYRINGE,7ML,TR/FR,RA,W/RES,-,P/G, Medline |
70084007 | SYRINGE,8ML,TR/FR,RA,W/RES,-,P/G, Medline |
70084017 | MTS,SYRINGE,8ML,TR/FR,RA,NO,RES,-,P/G, Medline |
80083007 | SYRINGE,7,ML,TR/FR,RA,W/RES,OEM,PG, Medline |
80084007 | SYRINGE,8,ML,TR/FR,RA,W/RES,OEM,PG, Medline |
80084017. | MTO,SYRINGE,8,ML,TR/FR,RA,NO,RES,OEM,PG, Medline |
- Amount recalled
- 192690 units
This recall covers 19 products
The agency filed one notice per product. You are reading one of them; the other 18 are below.
6 more are in the archive.
Where it was sold
Why it was recalled
Stop using this product now
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.
Using this product could cause serious injury, illness or death — stop using it now.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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