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 PACK
    • Medline SKU # DYNJ58475F
    • 2. URO/GEN ROBOTIC PACK
    • Medline SKU # DYNJ60803J
Lot codes and dates

18 of 18 products

Products covered by this recall
Model / numberBarcodesProduct 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.

Want the full recall guide?

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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:40 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.