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

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

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

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. 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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