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
16/01/2017 SynchroMed® II Implantable Infusion Pumps. Priority 2 – Warning Warning
04/01/2017 Summary of Field Safety Notices - December 2016 3rd Party Publications
21/12/2016 Life-Point Pro AED / bPLUS / mPLUS defibrillator devices and Adult Electrode Pads & Paediatric Electrode Pads. Priority 1 – Immediate Action For Immediate Action
15/12/2016 LMA® Mucosal Atomization Devices and LMA® MAD Nasal™ Intranasal Mucosal Atomization Devices. Priority 2 – Warning Warning
13/12/2016 Reflection Dead Blow Mallet. Priority 2 – Warning Warning
13/12/2016 Immucor Gamma Kleihauer Kit. Priority 2 – Warning Warning
13/12/2016 TOP-Q Super Fine Line TOP-Q Super Derm Line- Priority 2 Warning Warning
09/12/2016 CME T34 Ambulatory Syringe Pumps. Priority 3 – Advisory Advisory
05/12/2016 Summary of Field Safety Notice – November 2016 3rd Party Publications
05/12/2016 Multiple Ortho Reagent Red Blood Cell (RRBC) Products & - Control Reagent Products containing Red Blood Cells. Priority 2 – Warning Warning
29/11/2016 Laerdal Suction Unit when used with the LSU NiMH Battery at low temperatures. Priority 2 – Warning Warning
10/11/2016 Accu-Chek Aviva Combo, Accu-Chek Mobile bGM system, Accu-Chek Spirit Combo, Accu-Chek Spirit and Spirit Combo insulin pump. Priority 3 – Advisory Advisory
03/11/2016 EasySept Hydro Plus. Product Codes: 54085193‐120ML EASYSEPT Hydro Plus Starter kit.. 51085192‐360ML EASYSEPT Hydro Plus. 54085194‐3x360ML EASYSEPT Hydro Plus. Priority 1 – Immediate Action For Immediate Action
02/11/2016 Summary of Field Safety Notices - October 2016 3rd Party Publications
26/10/2016 LIFEPAK 1000 Defibrillator. Priority 2 – Warning Warning
26/10/2016 LIFEPAK CR Plus AED and LIFEPAK EXPRESS AEDs. Priority 2 – Warning Warning
18/10/2016 Liko® Viking® L, Viking® M, Viking® XL, and Viking® 300 Mobile Lifts. Priority 2 – Warning Warning
13/10/2016 Implantable Cardioverter Defibrillator: St. Jude Medical Fortify™, Fortify Assura™, Quadra Assura™, Quadra Assura MP™, Unify™, Unify Assura™ and Unify Quadra™. Priority 1 – For Immediate Action For Immediate Action
12/10/2016 Use of Luer adaptors with Needle-free Connection Systems and Glass Pre-filled Syringes. Priority 2 – Warning Warning
06/10/2016 Animas Vibe Insulin Infusion Pumps. Priority 2 – Warning Warning