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
21/02/2014 ARCHITECT Intact PTH Assay Reagents, Calibrators and Controls Advisory
21/02/2014 FreeStyle Mini® and FreeStyle® Blood Glucose Monitoring Systems Advisory
20/02/2014 Puma, Beatle, Alex & Ibis XP Power Wheelchairs Advisory
19/02/2014 Kodak 2100 and 2200 Advisory
11/02/2014 MINISEND-LUER LOCK CAP Advisory
11/02/2014 BD Plastipak™ 50mL Luer Lok Syringes with Syringe Pumps Advisory
04/02/2014 Field Safety Notice Monthly Summary Sheet - January 2014 3rd Party Publications
02/01/2014 Field Safety Notice Monthly Summary Sheet - December 2013 3rd Party Publications
17/12/2013 Patterson Walking Sticks - 404 Model Advisory
17/12/2013 Patterson Walking Frames (wheeled and non-wheeled) Advisory
04/12/2013 Field Safety Notice Monthly Summary Sheet - November 2013 3rd Party Publications
04/12/2013 FreeStyle Lite® Test Strips Recall
08/11/2013 NIPPY 3 ventilator, NIPPY JUNIOR ventilator, NIPPY ST ventilator, NIPPY S ventilator Advisory
01/11/2013 Field Safety Notice Monthly Summary Sheet - October 2013 3rd Party Publications
02/10/2013 Field Safety Notice Monthly Summary Sheet - September 2013 3rd Party Publications
18/09/2013 Zimma Walking Frames fitted with Wheeled Extension Legs Advisory
17/09/2013 Birdie & Flamingo Patient Lifters Advisory
03/09/2013 Field Safety Notice Monthly Summary Sheet - August 2013 3rd Party Publications
02/09/2013 HeartStart XL with M3516A batteries of lot number prefix ‘LK’ Advisory
20/08/2013 GlucoMen LX Sensor blood glucose test strips 50 count (product code 38877), used with the GlucoMen LX and GlucoMen LX PLUS meter Recall