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OFFICIAL-SOURCE RECALL · UNITED KINGDOM

Kimal Procedure Packs containing recalled components: Namic Recall: Medline Industries LP and Kimal PLC have

Use the identifiers printed on your item to determine whether this recall may affect the product you own.

CountryUnited KingdomPublishedMay 19, 2026Last updatedMay 22, 2026Official source last checkedSeptember 9, 2026 at 1:48 PM UTC

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Is your product affected?

Brand
See official notice
Product
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 use in urgent procedures where there are no alternatives. (DSI/2026/002)
Manufacturer
See official notice

The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.

Why this product was recalled

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.

Hazard

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.

What consumers should do

for the standalone syringe with the previous FSNs of syringe-containing procedure packs. For the Namic manifold, the updated FSN is to further clarify the safety

Official recall notice

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 use in urgent procedures where there are no alternatives. (DSI/2026/002)

Agency: Medicines and Healthcare products Regulatory Agency

Official publication date: May 19, 2026

Read the official UK_MHRA recall notice →

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