Safety communications

This page is for patients, the public and healthcare professionals.

It describes the different communications issued for device safety issues.

How is device safety information communicated?

There are two main types of safety communications:

  1. Field safety notices (FSNs), published by manufacturers.
  2. HPRA safety notices (SNs), published by us.

For more details on these communications, click the menu below. 

Field safety notices

Manufacturers must inform device users if they find a safety issue with their device.

Manufacturers issue FSNs to device users if they find a safety issue.

If your device is affected by a safety issue and you receive a FSN, read it carefully and follow the instructions.

FSNs may have key information or actions, such as:

  • Removal of a device from the market.
  • Updated instructions on how to use a device safely.
  • A patient recall (where patients are to be brought back for re-testing).

We publish a summary of FSNs affecting the Irish market during the first week of each month.

We also publish a list of FSNs circulated to the Irish market where actions remain outstanding.

We can only publish FSNs notified to us.

If you receive an FSN not on our list, please let us know by email at devicesafety@hpra.ie.

 

 

HPRA safety notices

If you receive a FSN from a manufacturer, act on it at once.

Do not wait for a HPRA safety notice . Most FSNs are not accompanied by a HPRA safety notice.

We issue HPRA safety notices to device users when we consider it necessary.

This includes:

  • To give more information to users in Ireland (FSNs often accompany SNs).
  • To raise awareness of a high risk FSN.
  • To raise awareness of an FSN where the manufacturer has not been able to contact all device users.
  • Where a company no longer exists.

More details on our safety notices, including how they are formatted, can be found here.

Anyone can sign up to receive HPRA safety notice by emailing devicesafety@hpra.ie.

What should I do if I receive a HPRA safety notice?

If you are a patient or member of the public, you should:

  • Review the safety notice.
  • Discuss any problems or concerns with your doctor.

If you are a healthcare professional, you should:

  • Ensure the notice reaches the correct person in your organisation.
  • Share the notice with other affected organisations or persons.
  • Review the notice and complete actions as needed.

 



Date Title Type
23/04/2012 G&S Smirthwaite Samba Chair Advisory
20/04/2012 Drive Medical Products - Drive WA007 Rollators, Drive Medical Nimbo Paediatric Walkers & Endres Riviera Bathlifts Advisory
04/04/2012 Field Safety Notice Monthly Summary Sheet - March 2012 3rd Party Publications
21/03/2012 Invacare Mobility Powerchairs Control Systems Advisory
01/03/2012 Field Safety Notice Monthly Summary Sheet - February 2012 3rd Party Publications
07/02/2012 Omnifuse and Omnifuse PCA Syringe Pumps Advisory
03/02/2012 Field Safety Notice Monthly Summary Sheet - January 2012 3rd Party Publications
06/01/2012 Field Safety Notice Monthly Summary Sheet - December 2011 3rd Party Publications
19/12/2011 Clinitest® hCG Advisory
19/12/2011 Femtosecond Laser System Advisory
09/12/2011 Quickie Neon Swing-Away Wheelchairs Advisory
08/12/2011 Action 3 and Action 4 Manual Wheelchairs Advisory
02/12/2011 Field Safety Notice Monthly Summary Sheet - November 2011 3rd Party Publications
01/12/2011 Birdie Patient Lifters Advisory
28/11/2011 Corona Medical Bed Side Rails – 1025, 1031 & SP 1027 Range Advisory
24/11/2011 Action® 2000 Manual Wheelchairs Advisory
22/11/2011 Reliant Lifter 100 / 150 / 200 / 250 Advisory
16/11/2011 Marus Brand LuxStar Dental Lights Advisory
11/11/2011 Storm3 Range (including Storm3 TT), Typhoon I & Typhoon II Power Wheelchairs Advisory
04/11/2011 Contoura® 880 Series Hospital Bed Frames Advisory