Ref: 2026/3296 - 5 June 2026
Important Customer Notice Status Update Type Product Recall
On 23 March 2026 the MHRA issued a Class 2 Medicine Recall, DMRC- 38814497 regarding Hibiwash 500ml bottle 4% Chlorhexidine Gluconate Antiseptic DEC85030.
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Ref: 2026/3349 - 3 June 2026
Important Customer Notice Status New Type Product Alert
Becton Dickinson (BD) has issued Field Safety Notice regarding BD Connecta™ Stopcocks.
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Ref: 2026/3345 - 3 June 2026
Important Customer Notice Status New Type Product Recall
Boston Scientific has issued Field Safety Notice 97593441-FA recalling CRETM Wireguided, CRE PROTM Wireguided, and CRE PRO GITM Wireguided balloon dilation catheters due to a potential sterile breach of the pouches in which the devices are packaged.
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Ref: 2026/3281 - 2 June 2026
Important Customer Notice Status Update Type Product Alert
Armstrong Medical has issued an update, Version 2, and provided further Instructions for Use, (IFUs) for their Field Safety Notice CAPA-100 to extend the scope of products affected.
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Ref: 2025/2802 - 28 May 2026
Important Customer Notice Status Update Type Supplier Update
The derogation with blood collection products from Greiner Bio-One is continuing.
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Ref: 2026/3326 - 28 May 2026
Important Customer Notice Status Update Type Product Recall
NHS England has also issued a communication dated 23 April 2026, publication reference: PRN02516.
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Ref: 2026/3342 - 26 May 2026
Important Customer Notice Status New Type Product Alert
Hamilton Medical has issued Field Safety Corrective Notice FSCA-2026-05-03 following post market surveillance highlighting an issue with certain breathing circuits set, coaxial.
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Ref: 2026/3335 - 21 May 2026
Important Customer Notice Status New Type Product Recall
Bayer has issued a Field Safety Notice SA-2026-RAD-03 regarding specific lots of the Multi-Patient Disposable Set used in conjunction with MEDRAD® Avanta Fluid Management Injection System.
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Ref: 2026/3333 - 13 May 2026
Important Customer Notice Status New Type Product Recall
Poly Medicure has issued a Field Safety Notice following reports of leakage of the Fannin IV Fluid Infusion Set during use. The leakage was observed at the junction between the Back Check Valve (BCV) and stopcock of the extension line.
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Ref: 2026/3314 - 7 May 2026
Important Customer Notice Status New Type Product Recall
Teleflex Arrow has issued a precautionary Field Safety Notice EIF-000605, recalling a number of Arrow Haemodialysis Kits and Sets.
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Ref: 2026/3328 - 5 May 2026
Important Customer Notice Status New Type Product Alert
Olympus has issued a Field Safety Notice FY26-006-F-1 to inform customers of an update to the instructions for use (IFU), for their ligating device MPC - N5382130.
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Ref: 2026/3311 - 21 April 2026
Important Customer Notice Status New Type Product Recall
Boston Scientific has issued Field Safety Notice 97251520D-FA initiating the recall of POLARx™ and POLARx™ Fit Cryoablation Balloon Catheters and POLARSHEATH™ Steerable Sheaths, and the decommissioning of SMARTFREEZE™ Cryoablation System consoles.
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Ref: 2025/2966 - 1 April 2026
Important Customer Notice Status Update Type Product Alert
We advised customers on the 30 May 2025 to quarantine four Open Suction Catheters supplied by GenX whilst we explore a potential issue.
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Ref: 2026/3301 - 31 March 2026
Important Customer Notice Status Update Type Product Recall
MOMA Foods is taking the precautionary step to expand their product recall to cover all MOMA Porridge and Cereal products on the market with a Best Before Date (BBE) between 24 April 2026 and 12 March 2027 due to potential contamination.
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Ref: 2026/3299 - 26 March 2026
Important Customer Notice Status Update Type Product Recall
GBUK has issued a Field Safety Notice regarding specific lots of Safety Hypodermic Needle 25G x 5/8" (0.5 x 16mm) Orange.
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