Ref: 2025/2977 - 5 June 2025
Important Customer Notice Status New Type Product Recall
Intersurgical has issued a Field Safety Notice regarding specific lots of i-View Video Laryngoscope having received reports of faulty devices resulting from depleted batteries.
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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: 2025/2960 - 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: 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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Ref: 2025/2824 - 23 April 2025
Important Customer Notice Status New Type Product Recall
Intersurgical Ltd has issued a Field Safety Notice following reports of the extendable expiratory gas tubing disconnecting from the T- piece, due to insecure connection of the two main parts.
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