FDA recall record

Ossur H / F LP Rotate Foot System prosthetic device for fitting lower extremity amputations. recall — FDA Z-1288-2015

The threads of the outer tube of the shock module of LP Rotate are too short, resulting in insecure assembly. Use of the product may cause the patient to…

Class IIclassification
Z-1288-2015official record ID
Mar 25, 2015report date

Recall record at a glance

Official recordZ-1288-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmOssur H / F
Report dateMar 25, 2015
Recall initiation dateMar 4, 2015
Quantity2,194 (1,464 in U.S. and 730 internationally)
LocationReykjavik, Iceland

Official product description

LP Rotate Foot System prosthetic device for fitting lower extremity amputations. -Low profile foot module with adjustable shock absorber and rotation with progressive stiffening -Build height: with male pyramid adapter 145 - 153mm (5 11/16 - 6 ) with female pyramid adapter 153 165mm (6 - 6 1/2) -Male pyramid adapter -Female pyramid adapter -Maintenance free, no lubrication required -Maximum weight: 147kg (325lbs) -Available in sizes 22-30

Why the product was recalled

The threads of the outer tube of the shock module of LP Rotate are too short, resulting in insecure assembly. Use of the product may cause the patient to fall with continued use, as the shock module can become loose from the foot blade.

Distribution information

Nationwide within the U.S. and internationally to the following foreign countries; Belgium, United Kingdom, Germany, Czech Republic, France, Israel, Poland, Spain, Australia, Japan, Mexico, Bulgaria, Canada, South Korea, Sweden, Finland,

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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