FDAJanuary 10, 2017device
LIMA Modular Revision Hip Stem Model 428-01-050_110 Product Usage: The Modular Revision Femoral hip stem is made up of a modular stem coupled with a proper neck by means of a Morse taper stabilized during the implantation phase by a safety screw. This system is particularly indicated for revision...
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Lima Proximal Bodies were inadvertently re-sterilized. The safety screw which affixes the distal and proximal bodies of the stem includes a thread-locking plug made from UHMWPE, which is not approved for repeated gamma sterilization.
What to do
FDA enforcement status: Terminated
Brands named
encore medical lpencoreencore medical
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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