FDASeptember 8, 2017device

Delta Cup Beater  Positioner - Aligner, model # 9057.20.555 Used during implantation of the Delta Acetabular System

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

An internal analysis on complaints received indicated that the welding process may have been performed sub optimally in the 12 lot # involved , leading to reduced mechanical strength of the device and possible breakage during impaction when the instrument is subjected to repeated multi-axial stresses.

What to do

FDA enforcement status: Completed

Brands named

limacorporate s p alimacorporate

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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