Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring
Pending LLM rewrite. Source: FDA_DEVICE Z-1726-2026.
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. ANGIO PACK, Medline SKU # DYNJ57032D; 2. NEURO INTERVENTIONAL RADIOLOGY, Medline SKU # DYNJ64026C; 3. NEURO INERVENTIONAL RADI
- 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 (20)
- Medline SKU # DYNJ57032D
- UDI/DI each 10198459183850
- UDI/DI case 40198459183851
- Lot Number: 25HBN999
- Lot Number: 25HBO039
- Medline SKU # DYNJ64026C
- UDI/DI each 10195327550059
- UDI/DI case 40195327550050
- Lot Number: 24JBC741
- Lot Number: 24IBM270
- Lot Number: 24IBE756
- Lot Number: 24GBC735
- Lot Number: 24FBF002
- Lot Number: 24DBC238
- Lot Number: 24ABY360
- Lot Number: 23LBH735
- Medline SKU # VASC1650
- UDI/DI each 10198459209666
- UDI/DI case 40198459209667
- Lot Number: 26ABP305
Distribution
Distributed nationwide across the United States.
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