MDA/2006/066 - Lancing devices used in nursing homes and care homes

Document details:

Type: Medical Device Alert
Series No: MDA/2006/066
Audience: Healthcare professionals
Published:
Format: Electronic and paper
Size: A4
Pages: 11
Price: free
ISBN/ISSN:
Author:
Copyright: Crown
   

1. Page 1

Update (April 2007): Correction to the list of disposable single-use lancing devices suitable for use in nursing homes and care homes (on page 2). Vitalcare Auto Safety Lancet is no longer available on prescription but Owen Mumford Ltd Unistik 3 range of lancets is now available on prescription instead.

 

Issued: 06 December 2006 at 11:00
Ref: MDA/2006/066


 

 

Immediate action
 
Action
Update
 
Information request


 

Device:
Lancing devices used in nursing homes and care homes.

>Page 2

Problem:
Transmission of hepatitis B between nursing home residents has been linked with the use of the wrong sort of lancing device. This has resulted in acute infections and deaths.

>Page 2

Action by:
Nursing home and care home staff.
 

Action:
For blood glucose monitoring nursing home and care home staff must only use:

  • disposable single-use lancing devices (these are used once and then the entire lancing device is discarded)
    or
  • a non-disposable lancing device which is intended for use on multiple patients and is used with disposable single-use lancets

>Pages 2-3

Distributed to:

NHS trusts in England - Chief Executives*
Commission for Social Care Inspection (CSCI) - Headquarters
Primary care trusts in England - Chief Executives*
Social services in England - Directors* 
Health Protection Agency (HPA)  - Directors

* via CE Bulletin

>Page 3

Contacts:
Details of MHRA contacts for technical and clinical aspects.
Change of address or removal from address list for CSCI.

>Pages 3-4

Appendix:
Extract from NHS PASA evaluation report 06002 Lancing Systems p25-31 (in pdf only).

>Pages 5-11



 

Action deadlines for the Safety Alert Broadcast System (SABS)
Deadline (action underway): 13 December 2006
Deadline (action complete): 02 January 2007


2. Page 2

Device:
A lancing device consists of a lancet and a firing mechanism.

  • In disposable single-use lancing devices the lancet and the firing mechanism are one unit and the entire device is disposed of after a single use.
  • Non-disposable lancing devices consist of disposable and reusable components. A single-use lancet is used on each occasion but the firing mechanism (often pen-like in design) is reusable. Lancing devices of this type are available which are intended for use on multiple patients. Careworkers and healthcare professionals should be aware that similar devices are also available for single patient self-monitoring and are often provided with a blood glucose meter purchased over the counter. Such lancing devices are not suitable for use on multiple patients.

Problem:
Two Medical Device Alerts have been issued about the transmission of hepatitis B linked to careworkers or healthcare professionals using the wrong type of lancing device to take blood samples in multi-patient environments (MDA/2004/044 and MDA/2005/063). These can be downloaded from the MHRA website http://www.mhra.gov.uk  > publications > safety warnings > medical device alerts.

MHRA continues to receive reports of hepatitis B outbreaks where the use of the wrong type of lancing device has been implicated in the transmission of the virus. These further reports all relate to nursing homes and care homes.

MHRA is issuing this further Medical Device Alert to reinforce the earlier advice, particularly to users of lancing devices in nursing homes and care homes.

Action:
Careworkers or healthcare professionals taking blood glucose samples in any multi-patient environment, including nursing homes and care homes must only use:

  • disposable single-use lancing devices for each resident or patient (these are used once and then the entire lancing device is discarded)
    or
  • a non-disposable lancing device, but this must be one which is intended to be used to take blood samples from multiple patients, used with disposable single-use lancets.

Nursing home and care home owners and all staff involved in the management and provision of lancing devices should ensure that the right devices are provided for taking blood samples in multi-patient environments. Examples of disposable single-use lancing devices and non-disposable lancing devices have been evaluated by the NHS Purchasing and Supply Agency Evaluation Report 06002 Lancing Systems. The devices evaluated in the report, which are suitable for testing patients in nursing homes and care homes, are listed below:

Disposable single-use lancing devices

  • HaeMedic Haemolance Plus
  • SurgiLance Safety Lancet
  • BD Genie Safety Lancet
  • HemoCue Safety Lancet
  • Owen Mumford Unistik 3
  • Roche Accu-Chek Safe-T-Pro Plus
  • Greiner Bio-One Vacuette Safety Lancet
  • VitalCare Auto Safety Lancet (this product is available on prescription)
  • Vitrex Safe Safety Lancet
  • ITC Tenderlett

3. Page 3

Action (continued):
Multi-patient non-disposable lancing devices

  • Bayer Glucolet 2 which uses Bayer Minilet single-use lancets
  • Roche Accu-Chek Softclix Pro which uses Roche Softclix Pro lancets (Note Roche Accuchek Softclix, Softclix II, Softclix Plus and Multiclix lancing devices are intended for self-use by one patient only to take blood samples for self-monitoring. They are not intended for use by healthcare or care workers to obtain blood samples from multiple patients).

Pages 25-31 of the evaluation report are appended to this Medical Device Alert (in pdf only). A full copy of the report can be downloaded from the PASA website at http://www.pasa.nhs.uk/evaluation > publications > pathology > blood glucose monitoring systems and lancing devices. Please note that this list is not exhaustive and that other products may also be suitable.

Distribution:
Please bring this notice to the attention of all who need to know or be aware of it. This will include
distribution by:

Trusts to:
SABS liaison officers for onward distribution to all relevant staff including:

  • Diabetes nurse specialists
  • Microbiologists

Primary care trusts to:
SABS liaison officers for onward distribution to all relevant staff including:

  • Community diabetes specialist nurses
  • Community nurses
  • Community pharmacists
  • Directors of public health
  • District nurses
  • General practitioners
  • Infection control nurses
  • Pharmaceutical advisors

Commission for Social Care Inspection (CSCI) to:
Headquarters for onward distribution to:

  • Adult placements
  • Care homes (adults, older people and children)
  • Care homes providing nursing care
  • Inspectors
  • Residential special schools

Social services to:
Liaison officers for onward distribution to all relevant staff including:

  • In-house residential care homes

Health Protection Agency to:
Directors for onward distribution to:

  • Consultants in communicable disease control
  • Health protection nurses

Contacts:
Enquiries to the MHRA should quote reference number 2006/009/012/291/010 and be addressed to:

Technical aspects: Clinical aspects:

Ainsley Wickens or Catriona Blake
Medicines & Healthcare products Regulatory Agency
Market Towers
1 Nine Elms Lane
London SW8 5NQ

Tel: 020 7084 3273/3219
Fax: 020 7084 3209

E-mail:
ainsley.wickens@mhra.gsi.gov.uk
catriona.blake@mhra.gsi.gov.uk

Jonathan Plumb
Medicines & Healthcare products Regulatory Agency
Market Towers
1 Nine Elms Lane
London SW8 5NQ

Tel: 020 7084 3128
Fax: 020 7084 3111

E-mail:
jonathan.plumb@mhra.gsi.gov.uk



Change of address or removal from address list for CSCI:
CSCI Customer Service Unit
St Nicholas Building
St Nicholas Street
Newcastle-upon-Tyne
NE1 1NB

Tel: 0845 015 0120

E-mail: enquiries@csci.gsi.gov.uk

4. Page 4

How to report adverse incidents
Incidents relating to medical devices must be reported to the Medicines and Healthcare products Regulatory Agency (MHRA) as soon as possible.

Further information about reporting incidents; online incident reporting facilities; and downloadable report forms are available from MHRA's website (http://www.mhra.gov.uk).

Alternatively, further information and printed incident report forms are available from:
MHRA Adverse Incident Centre
Medicines and Healthcare products Regulatory Agency
Market Towers, 1 Nine Elms Lane, London SW8 5NQ
Telephone 020 7084 3080 or Fax 020 7084 3109
or e-mail: aic@mhra.gsi.gov.uk
(An answerphone service operates outside normal officer hours)

Medical Device Alerts are available in full text on the MHRA website: http://www.mhra.gov.uk

Further information about SABS can be found at www.info.doh.gov.uk/sar/cmopatie.nsf

 

Page last modified: 06 December 2006