Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:18538
Brand Name:Ossur LP rotate, sizes 25-27 cat.1-6
Model:Product numbers LRP062, LRF062, LRPU62, and LRFU62
Affected:Manufacturing Lot Number: HF141022
Software version:
Recalling Organisation:Christchurch Artificial Limb Centre
330 Burwood Road
Christchurch 8083
Contact Information:0508 383 383
Manufacturer:Ossur HF
Issue:Ossur is recalling this device due to the outer tube threads not being machined correctly. Use of the affected product may cause the patient to fall, as the shock module can become loose from the foot blade. The failure could possibly be noticed by users as they will feel looseness on ankle foot device. If use is continued, connection of shock adapter to foot blade might break and user may fall.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Sponsor Control
Date Commenced:23/7/2015
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