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?

8 of 8 products

Products covered by this recall
Model / numberBarcodesProduct as published
VASC10611088994246472240889942464723Medline , UDI/DI each 10889942464722, UDI/DI case 40889942464723, Lot Number 25IBN161
VASC10611088994246472240889942464723Medline , UDI/DI each 10889942464722, UDI/DI case 40889942464723, Lot Number 25GBF769
VASC10741088994261175140889942611752Medline , UDI/DI each 10889942611751, UDI/DI case 40889942611752, Lot Number 25HBN798
VASC10741088994261175140889942611752Medline , UDI/DI each 10889942611751, UDI/DI case 40889942611752, Lot Number 25GBL527
VASC11981019348966426340193489664264Medline , UDI/DI each 10193489664263, UDI/DI case 40193489664264, Lot Number 25GDA142
VASCSHPOFF11088994240550340889942405504Medline , UDI/DI each 10889942405503, UDI/DI case 40889942405504, Lot Number 25IBP989
VASCSHPOFF11088994240550340889942405504Medline , UDI/DI each 10889942405503, UDI/DI case 40889942405504, Lot Number 25GBL526
VASCSLPON11088994240551040889942405511Medline , UDI/DI each 10889942405510, UDI/DI case 40889942405511, Lot Number 25GBL070.
Amount recalled
1698 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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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.