Kimal Procedure Packs Containing Recalled Components: Namic Angiographic Syringe With The Risk Of Syringe Disconnection; Namic Manifolds With The Risk Of Foreign Particulates. Important Guidance For U

Recall Summary Kimal Procedure Packs containing certain Namic syringes and manifolds are being recalled due to two safety issues: the angiographic syringes may disconnect during use, and the manifolds may contain foreign particles. The recall affects hospitals in the United Kingdom, and manufacturers advise these products should not be used except in emergency situations where no alternatives are available.

Reason
Medline Industries LP and Kimal PLC have identified safety issues with the Namic Angiographic Control Syringes with RA and Namic White Star Off Handle Manifold devices, and have issued field safety notices to affected UK hospitals advising that they should not be used except in urgent procedures where there are no alternatives.
Classification
Unclassified
Category
drug recall
Country
United Kingdom
Agency
UK Medicines and Healthcare products Regulatory Agency
Recall date
2026-05-22
Status
Ongoing
Distribution
United Kingdom

Official recall notice from UK Medicines and Healthcare products Regulatory Agency

Recall details on Nibble Recalls: https://trynibble.app/recalls/c8d294e1-d33b-4d91-bb51-cf4a01715e92