[pending] Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring
Pending LLM rewrite. Source: FDA_DEVICE Z-1726-2026.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: Pending LLM scoring against the rubric.
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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