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?

23 of 23 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ57032D1019845918385040198459183851Medline , UDI/DI each 10198459183850, UDI/DI case 40198459183851, Lot Number: 25HBN999
DYNJ57032D1019845918385040198459183851Medline , UDI/DI each 10198459183850, UDI/DI case 40198459183851, Lot Number: 25HBO039
DYNJ64026C1019532755005940195327550050Medline , UDI/DI each 10195327550059, UDI/DI case 40195327550050, Lot Number: 24JBC741
DYNJ64026C1019532755005940195327550050Medline , UDI/DI each 10195327550059, UDI/DI case 40195327550050, Lot Number: 24IBM270
DYNJ64026C1019532755005940195327550050Medline , UDI/DI each 10195327550059, UDI/DI case 40195327550050, Lot Number: 24IBE756
DYNJ64026C1019532755005940195327550050Medline , UDI/DI each 10195327550059, UDI/DI case 40195327550050, Lot Number: 24GBC735
DYNJ64026C1019532755005940195327550050Medline , UDI/DI each 10195327550059, UDI/DI case 40195327550050, Lot Number: 24FBF002
DYNJ64026C1019532755005940195327550050Medline , UDI/DI each 10195327550059, UDI/DI case 40195327550050, Lot Number: 24DBC238
DYNJ64026C1019532755005940195327550050Medline , UDI/DI each 10195327550059, UDI/DI case 40195327550050, Lot Number: 24ABY360
DYNJ64026C1019532755005940195327550050Medline , UDI/DI each 10195327550059, UDI/DI case 40195327550050, Lot Number: 23LBH735
VASC16501019845920966640198459209667Medline , UDI/DI each 10198459209666, UDI/DI case 40198459209667, Lot Number: 26ABP305
VASC16501019845920966640198459209667Medline , UDI/DI each 10198459209666, UDI/DI case 40198459209667, Lot Number: 26ABI725
VASC16501019845920966640198459209667Medline , UDI/DI each 10198459209666, UDI/DI case 40198459209667, Lot Number: 25KBD893
VASC16501019845920966640198459209667Medline , UDI/DI each 10198459209666, UDI/DI case 40198459209667, Lot Number: 25HBM531
VASC16501019845920966640198459209667Medline , UDI/DI each 10198459209666, UDI/DI case 40198459209667, Lot Number: 25HBA055
VASC16501019845920966640198459209667Medline , UDI/DI each 10198459209666, UDI/DI case 40198459209667, Lot Number: 25EBC929
VASC16501019845920966640198459209667Medline , UDI/DI each 10198459209666, UDI/DI case 40198459209667, Lot Number: 25DBL096
VASC16501019845920966640198459209667Medline , UDI/DI each 10198459209666, UDI/DI case 40198459209667, Lot Number: 25DBD577
VASC16501019845920966640198459209667Medline , UDI/DI each 10198459209666, UDI/DI case 40198459209667, Lot Number: 25DBI493
VASC16501019845920966640198459209667Medline , UDI/DI each 10198459209666, UDI/DI case 40198459209667, Lot Number: 25ABI074
Amount recalled
2154 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.

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, 6:20 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.