Reported Apr 15, 2026 · Ongoing
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA…
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?
- Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes)
- labeled as follows
1. DELIVERY PACKMedline SKU # DYNJ42892F2. DELIVERY PACKMedline SKU # DYNJ42892G
- Lot codes and dates
13 of 13 products
Products covered by this recall Model / number Barcodes Product as published DYNJ42892F40195327693719Medline , UDI/DI each10195327693718, UDI/DI case 40195327693719, Lot Number : 25GMD696 DYNJ42892F40195327693719Medline , UDI/DI each10195327693718, UDI/DI case 40195327693719, Lot Number : 25EMJ573 DYNJ42892F40195327693719Medline , UDI/DI each10195327693718, UDI/DI case 40195327693719, Lot Number : 25DMC646 DYNJ42892F40195327693719Medline , UDI/DI each10195327693718, UDI/DI case 40195327693719, Lot Number : 25BMD630 DYNJ42892F40195327693719Medline , UDI/DI each10195327693718, UDI/DI case 40195327693719, Lot Number : 24LMA523 DYNJ42892F40195327693719Medline , UDI/DI each10195327693718, UDI/DI case 40195327693719, Lot Number : 24KMA084 DYNJ42892F40195327693719Medline , UDI/DI each10195327693718, UDI/DI case 40195327693719, Lot Number : 24JME306 DYNJ42892F40195327693719Medline , UDI/DI each10195327693718, UDI/DI case 40195327693719, Lot Number : 24FME624 DYNJ42892F40195327693719Medline , UDI/DI each10195327693718, UDI/DI case 40195327693719, Lot Number : 24EMF099 DYNJ42892G40198459504571Medline , UDI/DI each10198459504570, UDI/DI case 40198459504571, Lot Number : 26BMH149 DYNJ42892G40198459504571Medline , UDI/DI each10198459504570, UDI/DI case 40198459504571, Lot Number : 26AMD029 DYNJ42892G40198459504571Medline , UDI/DI each10198459504570, UDI/DI case 40198459504571, Lot Number : 25KMA060 DYNJ42892G40198459504571Medline , UDI/DI each10198459504570, UDI/DI case 40198459504571, Lot Number : 25IMA514. - Amount recalled
- 966 kits
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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