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Australian Pharmaceutical Industries (API), in consultation with the TGA, has initiated a recall of certain models of their Forearm Crutch following reports of injuries after falling or slipping while using the product.
The glue used to secure the plastic handgrip to the handle may have been defective meaning the hand grip on the Forearm Crutch is not securely affixed. This might cause it to slide out from the length of the steel handle and detach from the crutch body.
The affected batch numbers are below:
| Product | Forearm Crutch Tall | Forearm Crutch Adult |
|---|---|---|
| Model Number | 251097 | 234354 |
| Batch Numbers | 251097-2105-1 251097-2107-1 251097-2201-1 | 234354-2105-1 234354-2107-1 234354-22-1-1 234354-2204-1 |
What should I do?
Check the red sticker on the crutch to confirm the model and batch number. If you have Forearm Crutches (Tall or Adult) with a batch number included in the table, immediately stop using the crutches and return them to the place of purchase for a refund.
Pharmacies, other retailers and wholesalers who have purchased this product are advised to inspect stock immediately and quarantine all units from the affected batches. All unsold units will be removed from the market by the sponsor.
Reporting problems
Consumers and health professionals are encouraged to report problems with medical devices. Your report will contribute to the TGA's monitoring of these products. For more information see the TGA Incident Reporting and Investigation Scheme (IRIS).
The TGA cannot give advice about an individual's medical condition. You are strongly encouraged to talk with a health professional if you are concerned about a possible adverse event associated with a medical device.