The Recall Desk
HighFDA (Devices)·Z-1722-2026·Announced 2026-04-15

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

Pending LLM rewrite. Source: FDA_DEVICE Z-1722-2026.

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. LAPAROSCOPIC HERNIORRHAPHY DSC, Medline SKU # DYNJ63021B; 2. LAP PACK, Medline SKU # DYNJ64297B; 3. MINOR PROCEDURE PACK, Medl
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 (9)

  • Medline SKU # DYNJ63021B
  • UDI/DI each 10193489833775UDI/DI case 40193489833776
  • Lot Number: 26AMD887
  • Medline SKU # DYNJ64297B
  • UDI/DI each 10198459472992UDI/DI case 40198459472993
  • Lot Number: 26AMA970
  • Medline SKU # DYNJ82411
  • UDI/DI each 10195327193232UDI/DI case 40195327193233
  • Lot Number: 25IMB049.

Distribution

Distributed nationwide across the United States.

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