FDAMarch 12, 2018device
Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation of fractures, joint contractures, fusions, limb lengthening, deformity correction, bone and soft tissue reconstruction in pediatric patients and adults.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The wrong parts were picked for packaging. The connecting Nuts were packed in the packaging labeled with Hinge coupling
What to do
FDA enforcement status: Terminated
Brands named
stryker
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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