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Manufacturers’ Field Safety Notices
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This message is sent to share information on manufacturers’ field safety notices (FSNs) which have been brought to our attention. Manufacturers have a legal duty to distribute these notices to affected customers.
This message does not affect the manufacturer’s FSN distribution, but it provides a reference source to check against.
You should always contact your supplier or the manufacturer if you are affected by a field safety notice listed below but have not received it from them. This will help ensure that you are not also missed from future FSN distributions. Note that field safety notices will only be listed in the sections below if we have been made aware of them.
Section 1 below lists selected FSNs and other relevant safety updates for estates, facilities or general products which have been brought to our attention through various sources including Office for Product Safety and Standards (OPSS). Section 2 lists FSNs for medical devices brought to our attention specifically by Medicines and Healthcare products Regulatory Agency (MHRA).
Section 1: estates, facilities or general products
None
Section 2: medical devices 25/12/23-29/12/23
- Beckman Coulter: iQ200 Series / DxU 850m/840m 45282 Urine analyser IVD, laboratory Model: iQ200 2G-60 MICROSCOPY MODULE, TESTED: 700-3320 iQ200 ELITE TESTED: 700-3370 iQ200 SELECT 2008 TESTED: 700-3345 iQ200 SELECT 2008 INSTRUMENT: 700-3347 iQ200 ELITE INSTRUMENT Non ROHS COMPLIANT: C10683 iQ200 ELITE 2008 TESTED: 700-3375 iQ200 SPRINT 2008 TESTED: 700-3325 iQ200 SELECT INSTRUMENT Non ROHS COMPLIANT: C10684 Instrument, DxU 850m Iris: C49513 Instrument, DxU 840m Iris: C76947 Rev 2 Flow Cell Capsule Spare: C04154 iQ Waste Well Adapter: 700-3393 iQ Clear Kit for iQ SPRINT: 800-3565 iQ Clear Kit for iQ SELECT: 800-3566 MHRA reference: 27752369
- Philips: Philips BrightView, X, XCT 45274 Full-body AMI system Model: 882480, 882478, 882482 MHRA reference: 27756859 2023/012/019/601/079
- Philips: Philips BrightView, X, XCT 45281 Model: 882480, 882478, 882482 MHRA reference: 27756301 2023/012/004/601/063
The above list of FSNs for medical devices is copied from the relevant MHRA web page. If you wish to browse or search for FSNs on the MHRA website, please click here.
Adverse Incidents
Incidents and near-misses should always be reported to local incident management systems (often referred to as Datix, Ullyses, SHE, etc.). However, IRIC also needs to be informed about incidents and near-misses when they involve:
- Medical devices, e.g. infusion pump, central line, hoist, care bed, x-ray machine, ventilator
- In vitro diagnostic devices or IVDs, e.g. blood analyser, reagent, SARS-CoV-2 test kit
- Estates and facilities, e.g. electrical installations, window restrictors, nurse call systems
- Social care equipment, e.g. mobile wheeled commode, powered rise and recline chair
- Personal protective equipment or PPE, e.g. visors, FFP3 respirators, aprons
We need incident reports so we can work with manufacturers and our partners to stop the same thing happening again. Health and care professionals can also report safety concerns about equipment and devices when an incident or near-miss has yet to occur. Information about how to report an incident to IRIC can be found here: https://www.nss.nhs.scot/health-facilities/incidents-and-alerts/report-an-incident/
Incident Reporting & Investigation Centre (IRIC)
Facilities Division
NHSScotland Assure
NHS National Services Scotland
Tel: 0131 275 7575|nss.iric@nhs.scot | Report an incident | Find safety alerts | IRIC | Turas Learn
We are NHS National Services Scotland. We offer a wide range of services and together we provide national solutions to improve the health and wellbeing of the people of Scotland. Find out more about our services at www.nss.nhs.scot
FAC406-212, 8B(i), Rev 6
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