Ref: 2025/2978 - 5 June 2025
Important Customer Notice Status New Type Product Alert
Drager has issued a Field Safety Notice regarding the slow increase of CO2-curve when using of the sampling port of Draeger Filter/HME for the products affected.
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Ref: 2025/2973 - 3 June 2025
Important Customer Notice Status New Type Product Alert
Rocket Medical has issued a Field Safety Notice, updating the Instructions For Use (IFU) for Rocket Copeland Fetal Scalp Electrodes.
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Ref: 2025/2966 - 30 May 2025
Important Customer Notice Status New Type Product Alert
NHS Supply Chain has made the decision to quarantine four Open Suction Catheters supplied by GenX whilst we explore a potential issue.
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Ref: 2025/2960 - 28 May 2025
Important Customer Notice Status New Type Product Recall
B Braun has issued a Field Safety Notice recalling specific batch numbers of Procedure Packs containing BD ChloraPrep™ 1ml.
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Ref: 2025/2954 - 21 May 2025
Important Customer Notice Status New Type Product Recall
Cook Medical has issued a Field Safety Notice dated 13 May 2025 regarding specific lots of Beacon® Tip 5.0 Fr Angiographic Catheters.
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Ref: 2025/2924 - 21 May 2025
Important Customer Notice Status New Type Product Alert
Medtronic has issued a Field Safety Notice regarding updates to the Instructions for Use (IFU) and Physician/Healthcare Practitioner Training related to potential damage to the bioprosthesis container (jar) upon opening.
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Ref: 2024/2723 - 21 May 2025
Important Customer Notice Status Update Type Product Recall
Becton Dickinson (BD) has issued an update to their Field Safety Notice (FSN), dated 15 May 2025, to include additional products and lots of affected 4Fr Single-Lumen PowerPICC Catheters (SOLO and non-SOLO versions).
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Ref: 2025/2945 - 16 May 2025
Important Customer Notice Status New Type Product Recall
Greiner Bio-One has issued a Customer Notification regarding a specific lot of product code KFK333 (Supplier Code 454322), Vacuette 2ml 3.2% Citrate 13 x 75mm Blue White Push Cap.
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Ref: 2025/2929 - 15 May 2025
Important Customer Notice Status New Type Product Alert
Philips has issued a Field Safety Notice: 2025-CC-HPM-011, updating the instructions for use, (IFU), for the Microstream Advance Intubated CO2 Filter Line, VitaLine Intubated CO2 Filter Line and FilterLine Intubated CO2 Filter Line.
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Ref: 2025/2934 - 14 May 2025
Important Customer Notice Status New Type Product Recall
Poly Medicure has instructed Fannin to quarantine two batches of the Autofusion Enhance IV sets as a precautionery measure following reports of the product not functioning as designed sporadically/randomly.
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Ref: 2025/2935 - 14 May 2025
Important Customer Notice Status New Type Product Alert
Salts Healthcare have been made aware that recent supplies of the Salts Adhesive Remover Spray (supplier code - WAP), may present with a stronger odour than usual of peppermint.
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Ref: 2025/2931 - 8 May 2025
Important Customer Notice Status New Type Product Recall
Solventum (our supplier KCI Medical) has issued a Field Safety Notice regarding 3M™ Prevena™ Plus 125 Therapy Unit and System Kits distributed between 11 March and 18 December 2024.
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Ref: 2025/2930 - 7 May 2025
Important Customer Notice Status New Type Product Recall
GBUK has issued a Field Safety Notice regarding specific lots of Arterial Cannula Kit 4Fr x 10cm.
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Ref: 2025/2918 - 6 May 2025
Important Customer Notice Status New Type Product Recall
Performance Health International has issued a Field Safety Notice having identified a limited number of Days adjustable standard crutches supplied since September 2024 that may contain defective handles due to a manufacturing error.
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Ref: 2025/2927 - 2 May 2025
Important Customer Notice Status New Type Product Alert
Johnson & Johnson has issued a Field Safety Notice regarding ENDOPATH ECHELON™ Vascular White Reload for Advanced Placement Tip (35 mm, 4 Row) product code VASECR35, distributed since 30 May 2024 and with expiration dates starting from 31 August 2026 to help ensure safe and effective use.
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