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Stryker GmbH recalls Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation of fractures, joint contractures, fusions, lim
Recalled May 2, 2018 · FDA recall Z-1526-2018 · Stryker
Hazard
The wrong parts were picked for packaging. The connecting Nuts were packed in the packaging labeled with Hinge coupling · FDA Class II
Units
18
Sold at
USA (nationwide) Distribution
Description
The wrong parts were picked for packaging. The connecting Nuts were packed in the packaging labeled with Hinge coupling
Product
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.
Manufacturer(s)
Stryker GmbH
Made in
Switzerland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →