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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Ref: 2025/2888 - 3 April 2025
Important Customer Notice Status New Type Product Alert
GBUK has issued an Advisory Field Safety Notice following discovery that two lot numbers, 241109 and 241119, have been transposed.
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Ref: 2025/2870 - 12 March 2025
Important Customer Notice Status New Type Product Alert
Vygon has issued an Advisory Field Safety Notice, to inform customers of an increase of customer reports in the UK relating to catheter fractures and malfunction of the pinch clamps on the catheter, specifically product code FSU129.
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Ref: 2025/2842 - 10 March 2025
Important Customer Notice Status Update Type Product Recall
The affected products remain impacted by the supply issue outlined in ICN 2759.
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Ref: 2025/2801 - 10 March 2025
Important Customer Notice Status Update Type Product Recall
Vygon has advised they are now able to fulfil orders of FSU373 with unaffected stock.
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Ref: 2025/2829 - 17 February 2025
Important Customer Notice Status New Type Product Recall
Medtronic has issued a Field Safety Notice initiating a product recall of the Pipeline Vantage devices with the part numbers PED3-027-xxx-xx, which represents compatibility to 0.027inch (0.69mm) inner diameter microcatheters “Pipeline Vantage 027”.
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Ref: 2025/2819 - 6 February 2025
Important Customer Notice Status New Type Product Recall
Zimmer Inc. is conducting a batch specific medical device Field Safety Corrective Action (removal) for seven batches of the NexGen LCCK Articular Surface with Locking Screw products.
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Ref: 2025/2810 - 29 January 2025
Important Customer Notice Status New Type Product Alert
Olympus has issued a Field Safety Notice following customer feedback reporting the probe tips of the Thunderbeat type S hand instruments becoming damaged or breaking, also instances of pad damage or breaking.
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