Angiographic Syringe Recall: Medline Industries Removes Namic Angiographic Rotating Adaptor Control Syringes

Published: 04/09/2026

Sources:
  • Food and Drug Administration
Relevant To:
  • Ambulatory Surgical Centers,
  • Rural Emergency Hospitals,
  • Dialysis Facilities,
  • Critical Access Hospitals,
  • Hospitals,
  • Ambulatory Care,
  • Inpatient Rehabilitation Facility

The FDA is aware that Medline Industries has issued an Urgent Medical Device Recall to affected customers recommending all Namic Angiographic Rotating Adaptor (RA) Control Syringes and Convenience Kits containing RA Syringes be removed from where they are used or sold. Affected devices:

  • Namic Angiographic Rotating Adaptor (RA) Control Syringes
  • Convenience Kits containing Namic Angiographic Rotating Adaptor (RA) Control Syringes  

Here is the list of affected products.

Medline Ind

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