HIGH

Medline Angiography Kit Recall: 3,120 Medical Convenience Kits With NAMIC Adaptor May Disconnect (Z-

Medline Industries, LP recalls 3,120 medical convenience kits worldwide due to a risk the syringe rotating adaptor may unwind during use. The issue can create a loose connection or complete disconnection between the syringe and manifold. The recall was issued on February 27, 2026 and is active. Customers should stop using the kit and follow manufacturer instructions for recall notices.

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

These kits are used to perform angiography procedures. They include syringes with NAMIC Angiographic Rotating Adaptor to connect syringes to a manifold.

Why This Is Dangerous

If the adaptor unwinds, it can create a loose or disconnected connection, potentially affecting sterile pathways during procedures.

Industry Context

This recall is not indicated as part of a broader pattern; it reflects post-market surveillance findings specific to this product line.

Real-World Impact

High risk during critical medical procedures; urgent action required to stop use and contact Medline for instructions.

Practical Guidance

How to identify if yours is affected

  1. Verify Medline SKU DYNJ42367B CVOR ANGIOGRAPHY PACK-LF
  2. Check UDIs 10193489211511 and case 40193489211512
  3. Inspect lot numbers for 24FBJ579, 24DBL828, 24DBE055, 24CBG967, 24ABN254, 23LBI540, 23KBF222, 23JBM761, 23JBA270, 23HBY791, 23HBD212, 23GBJ794, 23FBK893, 23EBQ313, 23DBC465

Where to find product info

FDA enforcement page Z-1714-2026 and Medline recall communications

What timeline to expect

Refunds or replacements are typically addressed within weeks to months after notification

If the manufacturer is unresponsive

  • Escalate to Medline customer service
  • File a report with the FDA if necessary
  • Consult healthcare provider for guidance

How to prevent similar issues

  • Verify supplier recalls before procurement
  • Maintain incident reporting with PPID
  • Use only calibrated NAMIC RA adaptors from authorized channels

Documentation advice

Keep recall notices, purchase records, and all communications; photograph kit and labels for records

Product Details

Medline medical convenience kits containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes. Labeled CVOR ANGIOGRAPHY PACK-LF, Medline SKU DYNJ42367B. Quantity: 3120 kits. Distribution: Worldwide, including US, Puerto Rico, and international markets (CA, NL, AU, KR, LK, PK, JP, AE, SG, SK).

Reported Incidents

No specific injuries or incidents are reported in the provided data.

Key Facts

  • 3120 kits recalled
  • Worldwide distribution including US and PR
  • Labeled CVOR ANGIOGRAPHY PACK-LF
  • Medline SKU DYNJ42367B
  • UDIs and multiple lot numbers listed
  • High risk following post-market surveillance
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
GENERALPREGNANTPETS
Injury Types
ELECTRICALLACERATIONOTHERSUFFOCATION

Product Classification

Product TypeAngiography Instrumentation/Syringes
Sold At
Unknown

Product Details

Model Numbers
Medline SKU DYNJ42367B UDI/DI each 10193489211511
UDI/DI case 40193489211512
Lot Numbers: 24FBJ579
24DBL828
24DBE055
+12 more
Affected States
ALL
Report Date
April 15, 2026
Recall Status
ACTIVE

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