The Recall Desk
SevereFDA (Devices)·Z-1718-2026·Announced 2026-04-15

NAMIC angiographic syringes recalled in the largest rotating adaptor action

Medline is recalling NAMIC Angiographic Syringes across multiple sizes because the rotating adaptor can unwind during use and disconnect from the manifold. 1,752,096 units are affected.

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 NAMIC Angiographic Syringes across multiple sizes and configurations, including Medline SKUs 70075027, 70085007, 70085107, 70087007 and others listed in the recall notice. The action covers 1,752,096 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 syringes are supplied to healthcare facilities rather than sold to consumers.

Facilities should identify affected stock using the Medline SKU, UDI and lot numbers in the recall notice, quarantine it, and follow the instructions issued by Medline. This is one of a series of related actions covering the same defect across standalone syringes and the convenience kits that contain them.

The recalled product

Product
NAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027; 2. SYRINGE,10ML,TR/FR,RA,W/RES, Medline SKU 70085007; 3. MTO,SYRINGE,10ML,TR/FG,RA,-,PKG, Medline SKU 70085107; 4. SYRINGE,12ML,TR/FR,RA,W/RES, Medline SKU 70087007; 5. MTO,SYRING
Manufacturer
Medline Industries, LP
Category
Medical Device — Angiographic syringe
Hazard
Affected units
1,752,096

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 # 60010027
  • UDI/DI each 10193489040166
  • UDI/DI case 30193489040160
  • Lot Number: 0000073035
  • Lot Number: 0000075896
  • Lot Number: 0000078648
  • Lot Number: 0000082387
  • Lot Number: 0000082384
  • Lot Number: 0000087087
  • Lot Number: 0000093180
  • Lot Number: 0000093741
  • Lot Number: 0000095735
  • Lot Number: 0000102248
  • Lot Number: 0000102694
  • Lot Number: 0000105537
  • Lot Number: 0000107947
  • Lot Number: 0000113756
  • Lot Number: 0000117610
  • Lot Number: 0000118566
  • Lot Number: 0000122251

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

See all →

Same hazard · disconnection risk

See all →