The Recall Desk
SevereFDA (Devices)·Z-1726-2026·Announced 2026-04-15

Medline angiography and neuro kits recalled over syringe adaptor disconnection

Medline is recalling Angio Pack and Neuro Interventional Radiology convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: FDA Class I recall, which the rubric floors at Severe; no death is reported in the source, so it does not escalate to Critical.

Plain-English summary

Medline Industries, LP is recalling medical convenience kits containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes. This action covers the ANGIO PACK, Medline SKU DYNJ57032D, and Neuro Interventional Radiology packs including Medline SKU DYNJ64026C, among others listed in the recall notice. The action covers 2,154 units.

Medline 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 the manifold. The FDA classified the action as Class I, its most serious classification.

Distribution was worldwide, covering the United States nationwide including Puerto Rico, and Canada, the Netherlands, Australia, the Republic of Korea, Sri Lanka, Pakistan, Japan, the United Arab Emirates, Singapore and Slovakia. The kits are supplied to healthcare facilities rather than sold to consumers.

Facilities should identify affected kits using the Medline SKU, UDI and lot numbers in the recall notice, quarantine any stock on hand, and follow the instructions issued by Medline.

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 — Angiography convenience kit
Hazard
Affected units
2,154

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.

The notice also names 2 states specifically:

Part of a larger recall action

This product is one of 19 recalled by Medline Industries, LP under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 19 products in this recall →

Related recalls

Same manufacturer · Medline Industries, LP

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Same hazard · disconnection risk

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