HIGH

Medline NAMIC Angiographic Syringe Recall Affects 17,902 Kits Worldwide (2026)

Medline Industries, LP recalls 17,902 medical convenience kits worldwide after post-market surveillance found a potential risk of the syringe rotating adaptor unwinding. The recall covers NAMIC Angiographic RA control syringes labeled in 10 Medline SKUs. Healthcare providers should stop use 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
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

Medline medical convenience kits bundle NAMIC angiographic components used in interventional cath lab procedures. These kits aid procedural setup and delivery of contrast or medications via angiographic systems.

Why This Is Dangerous

The adaptor may unwind, loosening the syringe-to-manifold connection. A loose or disconnected connection can compromise device integrity during procedures.

Industry Context

This recall is part of post-market surveillance in medical devices. Not described as a broader pattern in the provided data.

Real-World Impact

Healthcare providers may need to halt certain procedures until replacement kits are obtained, potentially affecting workflow and patient safety.

Practical Guidance

How to identify if yours is affected

  1. Identify affected NAMIC RA syringe kits within Medline SKUs listed.
  2. Check UDI codes 10193489297393 and case code 40193489297394.
  3. Review lot numbers 24BBI341, 23LBP066, 23KBS305, 23JBA062, 23HBR594.

Where to find product info

Recall notices from Medline and FDA enforcement page Z-1716-2026. Manufacturer communications will include instructions.

What timeline to expect

Refunds or replacements typically processed within weeks; follow manufacturer's instructions for next steps.

If the manufacturer is unresponsive

  • Escalate to hospital risk management.
  • File a report with the local medical device regulator if necessary.
  • Document all communications and preserve the recalled kits as instructed.

How to prevent similar issues

  • Verify SKUs and UDIs before purchasing interventional kits.
  • Maintain an inventory control process to isolate recalled lots.
  • Establish alternate suppliers for critical angiography components.

Documentation advice

Document model numbers, lot numbers, UDI, purchase records, and all recall communications.

Product Details

Recall involves NAMIC Angiographic Rotating Adaptor control syringes included in Medline medical convenience kits. Distribution spans US, PR, and international markets including CA, NL, AU, KR, LK, PK, JP, AE, SG, SK. 10 Medline SKUs listed. 17902 kits recalled. Recall date 2026-02-27. Report date 2026-04-15.

Reported Incidents

No specific injuries or incidents are provided in the recall notice. The hazard is described as a potential risk identified through surveillance.

Key Facts

  • 17902 kits recalled worldwide
  • 10 Medline SKUs affected
  • Syringe RA adaptor unwinding risk
  • Loose connection or disconnection between syringe and manifold
  • Class I recall
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
GENERALPREGNANTPREGNANT
Injury Types
ELECTRICALCRUSHINGOTHER

Product Classification

Product TypeNAMIC Angiographic Rotating Adaptor (RA) Control Syringes
Sold At
Multiple Retailers

Product Details

Model Numbers
Medline SKU 00-HCT055P
UDI/DI each 10193489297393
UDI/DI case 40193489297394
Lot Number 24BBI341
Lot Number 23LBP066
+3 more
Affected States
ALL
Report Date
April 15, 2026
Recall Status
ACTIVE

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