HIGH

Medline NAMIC Angiographic Rotating Adaptor Syringes Recalled in 2,980 Kits Worldwide

Medline Industries, LP recalls 2,980 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall spans the United States, Puerto Rico and multiple international countries. The rotatable adaptor may unwind during use, risking a loose connection or disconnection between syringe and manifold. Patients and healthcare providers should stop using the device and followMed

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

NAMIC Angiographic Rotating Adaptor syringes are used in angiographic procedures to connect syringe to a manifold. These are packaged in medical convenience kits.

Why This Is Dangerous

The adaptor could unwind during use, causing a loose connection or full disconnection between syringe and manifold, potentially compromising sterile technique or introducing leaks.

Industry Context

This recall is not described as part of a broader industry pattern in the provided data.

Real-World Impact

The recall affects patient safety during interventional procedures and may require kit replacement during clinical workflows.

Practical Guidance

How to identify if yours is affected

  1. Locate Medline SKUs DYNJ68037C, DYNJ89845, DYNJ89845A in your stock or records
  2. Check associated UDI numbers and lot codes listed in the recall documents
  3. Verify packaging and labeling against recall notice

Where to find product info

FDA enforcement page Z-1719-2026; Medline recall communications with physicians and distributors

What timeline to expect

Refunds or replacements to be arranged through Medline recall process; timelines not specified in the provided data

If the manufacturer is unresponsive

  • Escalate to hospital purchasing department
  • File a complaint with Medline corporate consumer safety
  • Contact FDA or CPSC recall information lines for guidance

How to prevent similar issues

  • Implement supplier lot tracking to detect affected lots quickly
  • Verify adaptor integrity before use in any angiography kit
  • Maintain sterile technique and immediate discard if adaptor appears unsecured
  • Stay updated with Medline recall alerts for future actions

Documentation advice

Keep recall notice, lot numbers, UDI codes, and correspondence with Medline; document kit disposal or replacement steps

Product Details

Medline medical convenience kits containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes. Labeled as: 1) NON VASCULAR PACK, Medline SKU DYNJ68037C; 2) VEIN, Medline SKU DYNJ89845; 3) VEIN, Medline SKU DYNJ89845A. Distributed worldwide including US, PR, CA, NL, AU, KR, LK, PK, JP, AE, SG, SK.

Reported Incidents

No specific incidents or injuries were detailed in the provided information. The recall is categorized as Class I with a high hazard designation.

Key Facts

  • Class I recall
  • 2,980 kits
  • Global distribution including US and PR
  • Medline SKU DYNJ68037C
  • Medline SKU DYNJ89845
  • Medline SKU DYNJ89845A
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
ELECTRICALLACERATIONSUFFOCATIONOTHER

Product Classification

Product TypeAngiographic Rotating Adaptor Syringe Kit
Sold At
Unknown

Product Details

Model Numbers
Medline SKU # DYNJ68037C
UDI/DI each 10198459239328
UDI/DI case 40198459239329
Lot Number: 25HBV397
Medline SKU # DYNJ89845
+9 more
Affected States
ALL
Report Date
April 15, 2026
Recall Status
ACTIVE

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