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Stryker Spine recalls Stryker Oasys Midline Occiput Plate-1) Small 2) Medium 3) Large 4) Large Long 5) Mini. Allows for positioning direct
Recalled August 28, 2013 · FDA recall Z-1976-2013 · Stryker Spine
Hazard
Stryker has received reports from customers indicating post-operative fracture of the pin that connects the tulip head to the plate body. · FDA Class I
Units
1536 units (US) 880 (Foreign)
Sold at
Nationwide Distribution.
Description
Stryker has received reports from customers indicating post-operative fracture of the pin that connects the tulip head to the plate body.
Product
Stryker Oasys Midline Occiput Plate-1) Small 2) Medium 3) Large 4) Large Long 5) Mini. Allows for positioning directly on the midline keel of the occiput.
Manufacturer(s)
Stryker Spine
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →