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?

105 of 105 products

Products covered by this recall
Model / numberBarcodesProduct as published
00-HCT055P1019348929739340193489297394Medline , UDI/DI each 10193489297393, UDI/DI case 40193489297394, Lot Number 24BBI341
00-HCT055P1019348929739340193489297394Medline , UDI/DI each 10193489297393, UDI/DI case 40193489297394, Lot Number 23LBP066
00-HCT055P1019348929739340193489297394Medline , UDI/DI each 10193489297393, UDI/DI case 40193489297394, Lot Number 23KBS305
00-HCT055P1019348929739340193489297394Medline , UDI/DI each 10193489297393, UDI/DI case 40193489297394, Lot Number 23JBA062
00-HCT055P1019348929739340193489297394Medline , UDI/DI each 10193489297393, UDI/DI case 40193489297394, Lot Number 23HBR594
00-HCT055P1019348929739340193489297394Medline , UDI/DI each 10193489297393, UDI/DI case 40193489297394, Lot Number 23DBR051
DYNJ0376230Q1019348975930340193489759304Medline , UDI/DI each 10193489759303, UDI/DI case 40193489759304, Lot Number 24ABO014
DYNJ0376230Q1019348975930340193489759304Medline , UDI/DI each 10193489759303, UDI/DI case 40193489759304, Lot Number 23KBW878
DYNJ0376230Q1019348975930340193489759304Medline , UDI/DI each 10193489759303, UDI/DI case 40193489759304, Lot Number 23HBP761
DYNJ0376230Q1019348975930340193489759304Medline , UDI/DI each 10193489759303, UDI/DI case 40193489759304, Lot Number 23FBW006
DYNJ0376230Q1019348975930340193489759304Medline , UDI/DI each 10193489759303, UDI/DI case 40193489759304, Lot Number 23DBF403
DYNJ23532C1019348946087240193489460873Medline , UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25KMD905
DYNJ23532C1019348946087240193489460873Medline , UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25IMD215
DYNJ23532C1019348946087240193489460873Medline , UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25GMI326
DYNJ23532C1019348946087240193489460873Medline , UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25FMI653
DYNJ23532C1019348946087240193489460873Medline , UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25EMH566
DYNJ23532C1019348946087240193489460873Medline , UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25DMI277
DYNJ23532C1019348946087240193489460873Medline , UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25AMI608
DYNJ23532C1019348946087240193489460873Medline , UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 24LMH838
DYNJ23532C1019348946087240193489460873Medline , UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 24LMB458
Amount recalled
17902 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.

Free recall alerts

Get alerted about new Medline Industries, LP recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:57 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.