The Recall Desk
HighFDA (Devices)·Z-1727-2026·Announced 2026-04-15

[pending] Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring

Pending LLM rewrite. Source: FDA_DEVICE Z-1727-2026.

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. DELIVERY PACK, Medline SKU # DYNJ42892F; 2. DELIVERY PACK, Medline SKU # DYNJ42892G.
Manufacturer
Medline Industries, LP

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 (19)

  • Medline SKU # DYNJ42892F
  • UDI/DI each10195327693718
  • UDI/DI case 40195327693719
  • Lot Number : 25GMD696
  • Lot Number : 25EMJ573
  • Lot Number : 25DMC646
  • Lot Number : 25BMD630
  • Lot Number : 24LMA523
  • Lot Number : 24KMA084
  • Lot Number : 24JME306
  • Lot Number : 24FME624
  • Lot Number : 24EMF099
  • Medline SKU # DYNJ42892G
  • UDI/DI each10198459504570
  • UDI/DI case 40198459504571
  • Lot Number : 26BMH149
  • Lot Number : 26AMD029
  • Lot Number : 25KMA060
  • Lot Number : 25IMA514.

Distribution

Distributed nationwide across the United States.