HIGH

Medline NAMIC Angiographic RA Syringes Recalled in 1698 Kits for Unwinding Adaptor Risk (2026)

Medline Industries, LP recalls 1,698 medical convenience kits worldwide over a potential unwind of the NAMIC Angiographic Rotating Adaptor during use. The risk could cause a loose connection or complete disconnection between the syringe and manifold. Healthcare providers and patients should stop using the affected kits immediately and follow recall instructions.

Quick Facts at a Glance

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

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

NAMIC Angiographic Rotating Adaptor syringes are used in angiography procedures to connect syringes to manifolds.

Why This Is Dangerous

An adaptor unwinding during use can loosen or disconnect the syringe from the manifold, potentially affecting sterile technique and patient safety.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

The recall affects 1,698 kits worldwide. Immediate action is required to prevent potential procedural complications.

Practical Guidance

How to identify if yours is affected

  1. Check SKU against VASC1061, VASC1074, VASC1198, VASCSHPOFF1, VASCSLPON1.
  2. Review lot numbers: 25IBN161, 25GBF769, 25HBN798, 25GBL527, 25GDA142.
  3. Verify UDI/DI details: per-kit and per-unit identifiers.

Where to find product info

FDA enforcement page Z-1715-2026 and Medline recall notices.

What timeline to expect

Remedies will be issued via notification; expect multiple channels. Replacement or refund timelines vary by institution.

If the manufacturer is unresponsive

  • Escalate to hospital procurement or regulatory affairs.
  • File a formal recall report with Medline and the FDA if delays occur.

How to prevent similar issues

  • Verify adaptor connections before use.
  • Inspect NAMIC RA syringe kits for secure fittings prior to procedures.
  • Implement supplier quality checks for future NAMIC kits.

Documentation advice

Save all recall notices, kit SKUs, lot numbers, and correspondence. Photograph labels and serials for records.

Product Details

Medline medical convenience kits containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes. Kits include: 1) CSTM MANIFOLD KIT - TITUS, Medline SKU VASC1061; 2) CSTM MANIFOLD KIT - FRYE, Medline SKU VASC1074; 3) CRYO EP MANIFOLD KIT, Medline SKU VASC1198; 4) MANIFOLD KIT - 500PSI OFF, Medline SKU VASCSHPOFF1; 5) MANIFOLD KIT LOW PRESSURE ON, Medline SKU VASCSLPON1. Distribution: Worldwide, including US, PR, CA, NL, AU, KR, LK, PK, JP, AE, SG, SK. Recall Date: 2026-02-27. Report Date: 2026-04-15. Status: ACTIVE.

Reported Incidents

No incident counts are provided in the available documentation. The recall classification is Class I with high hazard level.

Key Facts

  • 1698 kits recalled
  • Syringe RA adaptor unwinds risk
  • Loose connection or disconnection between syringe and manifold
  • Worldwide distribution including US and PR; CA, NL, AU, KR, LK, PK, JP, AE, SG, SK
  • Recall date 2026-02-27
  • Report date 2026-04-15
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
GENERALPREGNANTPREGNANTPREGNANTPREGNANTPETS
Injury Types
ELECTRICALLACERATIONOTHERSUFFOCATION

Product Classification

Product TypeAngiographic Rotating Adaptor (RA) Control Syringes
Sold At
Multiple RetailersUnknown

Product Details

Model Numbers
Medline SKU VASC1061
UDI/DI each 10889942464722
UDI/DI case 40889942464723
Lot Number 25IBN161
Lot Number 25GBF769
+9 more
Affected States
ALL
Report Date
April 15, 2026
Recall Status
ACTIVE

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