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
| Model / number | Barcodes | Product as published |
|---|---|---|
00-HCT055P | 1019348929739340193489297394 | Medline , UDI/DI each 10193489297393, UDI/DI case 40193489297394, Lot Number 24BBI341 |
00-HCT055P | 1019348929739340193489297394 | Medline , UDI/DI each 10193489297393, UDI/DI case 40193489297394, Lot Number 23LBP066 |
00-HCT055P | 1019348929739340193489297394 | Medline , UDI/DI each 10193489297393, UDI/DI case 40193489297394, Lot Number 23KBS305 |
00-HCT055P | 1019348929739340193489297394 | Medline , UDI/DI each 10193489297393, UDI/DI case 40193489297394, Lot Number 23JBA062 |
00-HCT055P | 1019348929739340193489297394 | Medline , UDI/DI each 10193489297393, UDI/DI case 40193489297394, Lot Number 23HBR594 |
00-HCT055P | 1019348929739340193489297394 | Medline , UDI/DI each 10193489297393, UDI/DI case 40193489297394, Lot Number 23DBR051 |
DYNJ0376230Q | 1019348975930340193489759304 | Medline , UDI/DI each 10193489759303, UDI/DI case 40193489759304, Lot Number 24ABO014 |
DYNJ0376230Q | 1019348975930340193489759304 | Medline , UDI/DI each 10193489759303, UDI/DI case 40193489759304, Lot Number 23KBW878 |
DYNJ0376230Q | 1019348975930340193489759304 | Medline , UDI/DI each 10193489759303, UDI/DI case 40193489759304, Lot Number 23HBP761 |
DYNJ0376230Q | 1019348975930340193489759304 | Medline , UDI/DI each 10193489759303, UDI/DI case 40193489759304, Lot Number 23FBW006 |
DYNJ0376230Q | 1019348975930340193489759304 | Medline , UDI/DI each 10193489759303, UDI/DI case 40193489759304, Lot Number 23DBF403 |
DYNJ23532C | 1019348946087240193489460873 | Medline , UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25KMD905 |
DYNJ23532C | 1019348946087240193489460873 | Medline , UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25IMD215 |
DYNJ23532C | 1019348946087240193489460873 | Medline , UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25GMI326 |
DYNJ23532C | 1019348946087240193489460873 | Medline , UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25FMI653 |
DYNJ23532C | 1019348946087240193489460873 | Medline , UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25EMH566 |
DYNJ23532C | 1019348946087240193489460873 | Medline , UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25DMI277 |
DYNJ23532C | 1019348946087240193489460873 | Medline , UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 25AMI608 |
DYNJ23532C | 1019348946087240193489460873 | Medline , UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number 24LMH838 |
DYNJ23532C | 1019348946087240193489460873 | Medline , 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.
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