Reported Apr 15, 2026 · Ongoing

NAMIC Angiographic Syringe, labeled as follows

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?

NAMIC Angiographic Syringe, labeled as follows

17 of 17 products

Products covered by this recall
Model / numberProduct as published
70075027SYRINGE,20ML,CONTROL,-,PKG, Medline
70085007SYRINGE,10ML,TR/FR,RA,W/RES, Medline
70085107MTO,SYRINGE,10ML,TR/FG,RA,-,PKG, Medline
70087007SYRINGE,12ML,TR/FR,RA,W/RES, Medline
70087107MTO,SYRINGE,12ML,TR/FG,RA,W/RES, Medline
70088007SYRINGE,12ML,TR/FR,RA,W/O,RES,-,PKG, Medline
70095007SYRINGE,10ML,PP/FR,RA,-,PKG, Medline
70095107SYRINGE,10ML,PP/FG,RA,-,PKG, Medline
70097007SYRINGE,12ML,W/RES,PP/FR,RA,PG, Medline
70097107SYRINGE,12ML,PP/FG,RA,W/RES,-,PKG, Medline
70098107SYRINGE,12ML,PP/FG,RA,W/O,RES, Medline
80075027SYRINGE,20ML,TR/FR,RA,OEM,PG, Medline
80085007SYRINGE,10ML,ANGIO,W/RA,-,OEM, Medline
80087007SYRINGE,12ML,TR/FR,RA,OEM, Medline
80095007SYRINGE,10ML,PP/FR,RA,-,OEM,-,PG, Medline
80095107SYRINGE,10ML,PP/FG,RA,OEM,PG, Medline
80097107SYRINGE,12ML,PP/FG,RA,-,OEM,-,PG, Medline
Lot codes and dates

305 of 305 products

Products covered by this recall
Model / numberBarcodesProduct as published
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000073035
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000075896
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000078648
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000082387
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000082384
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000087087
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000093180
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000093741
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000095735
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000102248
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000102694
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000105537
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000107947
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000113756
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000117610
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000118566
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000122251
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000124476
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000126969
600100271019348904016630193489040160Medline , UDI/DI each 10193489040166, UDI/DI case 30193489040160, Lot Number: 0000131544
Amount recalled
1752096 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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By hazard

Other recalls from Medline Industries, LP

36 in total.

Where it was distributed

All recall categories · Browse the whole archive

Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:42 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.