One Liners issue 59 - June 2008

On the shelf
Poor storage and transport of walking frames, sticks and crutches has caused damage to the main support tubes which subsequently collapse during use.

• Walking sticks and frames require careful storage before issue and between periods of use to prevent them from sustaining structural damage.

tr-ACEABILITY
Walking aids were recalled by the manufacturer due to failures in use and staff in the local stores were unable to identify which users had been supplied with them to arrange replacement.

• Ensure that all receipts from the manufacturer and issues to the end user are recorded to allow traceability.

Get a grip
Some wheeled walking frames have hand operated braking systems which can be difficult to operate for some users.

• Ensure all users have enough strength and dexterity to operate the brakes before issue or seek alternative models.

An IFU is for Life, not just for Christmas
Some users are not aware how to use a walking aid properly; how to clean it, frequently check it for wear or damage and when to seek a replacement.

• Always ensure that a copy of the manufacturer’s Instructions For Use are issued to the user with every walking aid and include the issuing authority contact details.

From Flaw to Floor
Surface dents, cracks or elongation of adjustment holes occurring during use can lead to the walking aid failing and users being injured from the subsequent fall.

• Issuing authorities and users should frequently check the walking aid for wear and damage and replace if necessary.

These aids are made for walking
Walking sticks and crutches have been damaged by being used as “levers” to open doors or move other equipment leading to later failure in use.

• Ensure users are aware that misuse can weaken the structure and lead to a fall.

Adverse incidents should be reported at the earliest opportunity.
We prefer to receive reports via the online reporting system on our website www.mhra.gov.uk
You may also use this online system to send an e-mail copy of your report to your medical device liaison officer.
We also have an adverse incident hotline: 020 7084 3080. You can find detailed reporting guidance on our website.

For general advice on AT safety related matters please call the MHRA Centre for AT on 01253 596000