Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring
Pending LLM rewrite. Source: FDA_DEVICE Z-1719-2026.
Severity not yet assessed
We have not scored this recall against our rubric yet, so we are not showing a severity rating or our usual guidance. The agency’s own notice below is the authoritative source — read it first.
Plain-English summary
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.
The recalled product
- Product
- Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. NON VASCULAR PACK, Medline SKU # DYNJ68037C; 2. VEIN, Medline SKU # DYNJ89845; 3. VEIN, Medline SKU # DYNJ89845A.
- Manufacturer
- Medline Industries, LP
- Category
- Medical Device — Devices
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (17)
- Medline SKU # DYNJ68037C
- UDI/DI each 10198459239328
- UDI/DI case 40198459239329
- Lot Number: 25HBV397
- Medline SKU # DYNJ89845
- UDI/DI each 10198459292460
- UDI/DI case 40198459292461
- Lot Number: 25CBU222
- Medline SKU # DYNJ89845A
- UDI/DI each 10198459490965
- UDI/DI case 40198459490966
- Lot Number: 26BBC195
- Lot Number: 26ABI611
- Lot Number: 25LBK402
- Lot Number: 25KBH371
- Lot Number: 25IBK975
- Lot Number: 25HBQ426.
Distribution
Distributed nationwide across the United States.
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