HIGH

Medline NAMIC Angiographic Rotating Adaptor Syringes Recalled in Class I Action for 79,843 Units

Medline Industries issued a Class I recall for 79,843 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The action covers worldwide distribution including the US and PR. The risk is a syringe adaptor unwinding during use, which may cause a loose connection or disconnection with the manifold. Stop using the device 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 NAMIC RA syringes are used in angiography and related surgical packs within extensive MEDLINE kits.

Why This Is Dangerous

The rotating adaptor could unwind, creating a loose connection or disconnection with the manifold and potentially affecting device performance.

Industry Context

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

Real-World Impact

Immediate halting of use for affected kits; potential impact on procedural accuracy and safety; costs related to replacement.

Practical Guidance

How to identify if yours is affected

  1. Identify Medline SKU numbers listed in the recall.
  2. Check UDI DI numbers 10193489040340 and 40193489040341.
  3. Inspect lot numbers 26BBI625, 26ABB718, 25JBJ140, 25HBF702, 25GBC747.

Where to find product info

FDA recall page and Medline notice; contact healthcare providers for guidance.

What timeline to expect

Replacement or refunds will be issued per Medline instructions; timeline not specified.

If the manufacturer is unresponsive

  • Escalate to hospital procurement or distributor.
  • Maintain documentation of attempts to contact Medline.

How to prevent similar issues

  • Verify syringe adaptor integrity before use.
  • Follow vendor instructions for replacement kits.
  • Track lot numbers during inventory management.

Documentation advice

Keep recall notice, purchase records, and any adverse event reports; photograph affected SKUs and lot codes.

Product Details

Recall involves NAMIC Angiographic Rotating Adaptor (RA) Control Syringes distributed within Medline medical convenience kits. 79843 units recalled. Medline SKU variants include 60010508 and numerous other SKUs listed in the recall. UDI/DI: 10193489040340 (per case) and 40193489040341 (per case). Lot numbers include 26BBI625, 26ABB718, 25JBJ140, 25HBF702, 25GBC747.

Reported Incidents

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

Key Facts

  • 79,843 units recalled
  • Worldwide distribution including US, PR and foreign countries (CA, NL, AU, KR, LK, PK, JP, AE, SG,SK
  • Syringe adaptor unwinding risk leads to loose/disconnected connections
  • UMIs: 10193489040340 (UDI/DI per case) and 40193489040341 (UDI/DI per case)
  • Lot numbers: 26BBI625, 26ABB718, 25JBJ140, 25HBF702, 25GBC747
  • Class I recall—highest risk category
View Original Recall on FDA - Medical Devices

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERALPREGNANTPREGNANTPETS
Injury Types
ELECTRICALLACERATIONPOISONINGSUFFOCATIONOTHER

Product Classification

Product TypeSyringe/Angiography Kit Adaptor
Sold At
Multiple Retailers

Product Details

Model Numbers
Medline SKU # 60010508
UDI/DI each 10193489040340
UDI/DI case 40193489040341
Lot Number: 26BBI625
Lot Number: 26ABB718
+3 more
Affected States
ALL
Report Date
April 15, 2026
Recall Status
ACTIVE

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