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. ROBOTIC PACKMedline SKU # DYNJ58475F2. URO/GEN ROBOTIC PACKMedline SKU # DYNJ60803J
- Lot codes and dates
18 of 18 products
Products covered by this recall Model / number Barcodes Product as published DYNJ58475F1019845957238840198459572389Medline , UDI/DI each 10198459572388, UDI/DI case 40198459572389, Lot Number: 25LMK173 DYNJ60803J1019532713882040195327138821Medline , UDI/DI each 10195327138820, UDI/DI case 40195327138821, Lot Number: 26BMA268 DYNJ60803J1019532713882040195327138821Medline , UDI/DI each 10195327138820, UDI/DI case 40195327138821, Lot Number: 26AMH928 DYNJ60803J1019532713882040195327138821Medline , UDI/DI each 10195327138820, UDI/DI case 40195327138821, Lot Number: 25EMD876 DYNJ60803J1019532713882040195327138821Medline , UDI/DI each 10195327138820, UDI/DI case 40195327138821, Lot Number: 25EMA519 DYNJ60803J1019532713882040195327138821Medline , UDI/DI each 10195327138820, UDI/DI case 40195327138821, Lot Number: 25DMA846 DYNJ60803J1019532713882040195327138821Medline , UDI/DI each 10195327138820, UDI/DI case 40195327138821, Lot Number: 25BMH004 DYNJ60803J1019532713882040195327138821Medline , UDI/DI each 10195327138820, UDI/DI case 40195327138821, Lot Number: 25BMA218 DYNJ60803J1019532713882040195327138821Medline , UDI/DI each 10195327138820, UDI/DI case 40195327138821, Lot Number: 24KMI208 DYNJ60803J1019532713882040195327138821Medline , UDI/DI each 10195327138820, UDI/DI case 40195327138821, Lot Number: 24KMC007 DYNJ60803J1019532713882040195327138821Medline , UDI/DI each 10195327138820, UDI/DI case 40195327138821, Lot Number: 24JMD850 DYNJ60803J1019532713882040195327138821Medline , UDI/DI each 10195327138820, UDI/DI case 40195327138821, Lot Number: 24IMI939 DYNJ60803J1019532713882040195327138821Medline , UDI/DI each 10195327138820, UDI/DI case 40195327138821, Lot Number: 24EDB694 DYNJ60803J1019532713882040195327138821Medline , UDI/DI each 10195327138820, UDI/DI case 40195327138821, Lot Number: 24DDB793 DYNJ60803J1019532713882040195327138821Medline , UDI/DI each 10195327138820, UDI/DI case 40195327138821, Lot Number: 24CDB207 DYNJ60803J1019532713882040195327138821Medline , UDI/DI each 10195327138820, UDI/DI case 40195327138821, Lot Number: 24BDB439 DYNJ60803J1019532713882040195327138821Medline , UDI/DI each 10195327138820, UDI/DI case 40195327138821, Lot Number: 23GDB756 DYNJ60803J1019532713882040195327138821Medline , UDI/DI each 10195327138820, UDI/DI case 40195327138821, Lot Number: 23GDA532. - Amount recalled
- 439 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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