Ref: 2024/2743 - 27 November 2024
Important Customer Notice Status New Type Product Recall
Pajunk has issued a Field Safety Notice having identified an issue with assembly during manufacture of the Rectal Sheath Block MPC 0731163-49 (product code FTR85093).
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Ref: 2024/2675 - 26 November 2024
Important Customer Notice Status Update Type Contractual Change
The contractual change due to a novation from Medline Scientific Limited to Sciquip Limited is continuing.
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Ref: 2024/2737 - 15 November 2024
Important Customer Notice Status New Type Product Recall
Rocket Medical has issued a Field Safety Notice having identified a manufacturing issue affecting specific Lot numbers for two Chest Drainage Devices.
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Ref: 2024/2734 - 12 November 2024
Important Customer Notice Status New Type Product Recall
Abbott Rapid Diagnostics has received a Field Safety Notice from Actim Oy the manufacturer of Actim® Partus Test, withdrawing one Lot number following stability testing showing the Lot number does not fulfil the required criteria.
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Ref: 2024/2707 - 11 November 2024
Important Customer Notice Status Update Type Product Recall
Ebrington Medical has issued an updated Field Safety Notice following discovery of the potential risk of contamination in additional Lots, therefore the scope of the recall has widened to include Lot number 2024.06 expiry date 2027.06.
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Ref: 2024/2715 - 6 November 2024
Important Customer Notice Status New Type Product Recall
Ideal Medical Solutions has issued a precautionery Field Safety Notice following a report of poor product performance.
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Ref: 2024/2730 - 5 November 2024
Important Customer Notice Status New Type Product Recall
Smith Medical has issued a Field Safety Notice affecting three endotracheal tube introducers having identified a potential for ingress of fluid into the device during reprocessing. The ingress takes place at the rear of the device between the end cap and the tube.
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Ref: 2024/2718 - 5 November 2024
Important Customer Notice Status New Type Product Recall
Advanced Medical Solutions (AMS) has issued a Field Safety Notice initiating a precautionary recall having become aware of a defect on primary packaging pouches, in which minor missing patches of Polyethylene have been detected.
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Ref: 2024/2731 - 5 November 2024
Important Customer Notice Status New Type Product Alert
Olympus has issued a Field Safety Notice having become aware that five lot numbers may be missing product identification and an expiration date on the sterile packaging.
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Ref: 2024/2689 - 17 October 2024
Important Customer Notice Status New Type Product Alert
NHS Supply Chain has been made aware of two Field Safety Notices issued by Baxter on 26 June 2024 and 26 September 2024, due to Baxter identifying that the Braun Thermoscan Pro 6000 ear thermometers issued between 15 September 2022 and 22 February 2024 were supplied with a compact disc (CD) containing an outdated version of the instructions for use (IFU).
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Ref: 2024/2690 - 10 October 2024
Important Customer Notice Status New Type Product Recall
Intersurgical Ltd has issued a Field Safety Notice following a customer report and subsequent investigation identified a potential safety concern with five of their 10mm resuscitation breathing systems for use with the Neopuff® Resuscitator.
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Ref: 2024/2688 - 7 October 2024
Important Customer Notice Status New Type Product Recall
Smith Medical has issued a Field Safety Notice having identified a potential issue with the packaging sterile seals on specific Nasopharyngeal Airway, Double Swivel Connector, 15mm Y Piece, Portex™ Orator Speaking Valve, Thermovent™ 1200 products packaged between 20 January 2021 and 27 August 2021.
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Ref: 2024/2621 - 30 September 2024
Important Customer Notice Status Update Type Product Alert
In July 2024, Medtronic issued an Urgent Field Safety Notice for McGRATH™ MAC Video Laryngoscopes, item codes 300-000-000, which were within their useful life of 5 years (Serial numbers 366170 to 405673).
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Ref: 2024/2682 - 26 September 2024
Important Customer Notice Status New Type Product Recall
Rocket Medical has issued a Field Safety Notice withdrawing a single Lot number of their 8fg Safety Needle having identified that during production the adhesive/glue used to secure the drainage line to the stitch plate was not correctly applied.
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Ref: 2024/2673 - 19 September 2024
Important Customer Notice Status New Type Product Recall
Ambu has issued a Field Safety Notice following complaints regarding the design of the product Ambu® VivaSight™ 2 DLT, specifically referring to a hyper angulation of the distal end of the double lumen tube.
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