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
| Model / number | Barcodes | Product as published |
|---|---|---|
DYNJ68037C | 1019845923932840198459239329 | Medline , UDI/DI each 10198459239328, UDI/DI case 40198459239329, Lot Number: 25HBV397 |
DYNJ89845 | 1019845929246040198459292461 | Medline , UDI/DI each 10198459292460, UDI/DI case 40198459292461, Lot Number: 25CBU222 |
DYNJ89845A | 1019845949096540198459490966 | Medline , UDI/DI each 10198459490965, UDI/DI case 40198459490966, Lot Number: 26BBC195 |
DYNJ89845A | 1019845949096540198459490966 | Medline , UDI/DI each 10198459490965, UDI/DI case 40198459490966, Lot Number: 26ABI611 |
DYNJ89845A | 1019845949096540198459490966 | Medline , UDI/DI each 10198459490965, UDI/DI case 40198459490966, Lot Number: 25LBK402 |
DYNJ89845A | 1019845949096540198459490966 | Medline , UDI/DI each 10198459490965, UDI/DI case 40198459490966, Lot Number: 25KBH371 |
DYNJ89845A | 1019845949096540198459490966 | Medline , UDI/DI each 10198459490965, UDI/DI case 40198459490966, Lot Number: 25IBK975 |
DYNJ89845A | 1019845949096540198459490966 | Medline , UDI/DI each 10198459490965, UDI/DI case 40198459490966, Lot Number: 25HBQ426. |
- Amount recalled
- 2980 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.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.