HIGH

Medline NAMIC Angiographic Adaptor Syringes Recalled in 439 Kits for Unwind Risk (2026)

Medline Industries, LP recalled 439 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall spans worldwide distribution including the US, Puerto Rico, and multiple international markets.

Quick Facts at a Glance

Recall Date
February 27, 2026
Hazard Level
HIGH
Brand
Medline Industries, LP
Category
Health & Personal Care
Sold At
Unknown
Geographic Scope
1 states
At-Risk Groups
GENERAL, PREGNANT, PETS

Hazard Information

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.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

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About This Product

Medical convenience kits containing NAMIC Angiographic Rotating Adaptor control syringes are used in interventional procedures to connect syringes to manifolds in angiography.

Why This Is Dangerous

A rotating adaptor that unwinds can create a loose or complete disconnection between syringe and manifold, risking leakage or device failure.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Immediate action required; health care providers must halt use to avoid potential complications and ensure patient safety.

Practical Guidance

How to identify if yours is affected

  1. Review Medline NAMIC RA control syringe kits in use.
  2. Check SKUs DYNJ58475F and DYNJ60803J.
  3. Inspect UDI codes and Lot Numbers 25LMK173, 26BMA268, 26AMH928, 25EMD876, 25EMA519.

Where to find product info

Refer to FDA enforcement page and Medline recall notices for documentation and steps.

What timeline to expect

Recall could involve replacement or refund processes; timelines vary by region and distributor.

If the manufacturer is unresponsive

  • Escalate to hospital risk management.
  • File a formal complaint with Medline and the appropriate health authority.
  • Seek assistance from procurement/supply chain managers.

How to prevent similar issues

  • Verify adaptor integrity before procedures.
  • Use only recommended NAMIC RA syringes with compatible manifolds.
  • Establish supplier recalls communication to ensure rapid notification.

Documentation advice

Document lot numbers, SKUs, dates of receipt, and communications with Medline or suppliers.

Product Details

Product: Medline NAMIC Angiographic Rotating Adaptor (RA) Control Syringes. SKUs: DYNJ58475F and DYNJ60803J. UDIs: 10198459572388; 40198459572389; 10195327138820; 40195327138821. Lot numbers: 25LMK173; 26BMA268; 26AMH928; 25EMD876; 25EMA519. Quantity: 439 kits. Sold globally, including US, PR, CA, NL, AU, KR, LK, PK, JP, AE, SG, SK.

Reported Incidents

No injuries or incidents have been reported in the provided data.

Key Facts

  • 439 kits recalled
  • Class I recall
  • Worldwide distribution including US and PR
  • Syringe adaptor unwind risk
  • Loosening or disconnection from manifold
  • Lot numbers: 25LMK173, 26BMA268, 26AMH928, 25EMD876, 25EMA519
View Original Recall on FDA - Medical Devices

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Safety Guide

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERALPREGNANTPETSPREGNANT
Injury Types
ELECTRICALLACERATIONOTHER

Product Classification

Product TypeAngiographic Rotating Adaptor (RA) Control Syringes
Sold At
Unknown

Product Details

Model Numbers
Medline SKU # DYNJ58475F
UDI/DI each 10198459572388
UDI/DI case 40198459572389
Lot Number: 25LMK173
Medline SKU # DYNJ60803J
+6 more
Affected States
ALL
Report Date
April 15, 2026
Recall Status
ACTIVE

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