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SEASPINE ORTHOPEDICS CORPORATION recalls Brand Name: Meridian Angled Awl Fixed Product Name: Angled Awl Fixed Model/Catalog Number: RA2-003015 Product Descrip
Recalled July 24, 2024 · FDA recall Z-2357-2024 · SEASPINE ORTHOPEDICS
Hazard
Insufficient weld around the cap component of the instrument is insufficient to withstand impaction forces. · FDA Class II
Units
100 units
Sold at
The product was distributed to the following US states: Nevada, Colorado, Texas, Washington, Indiana, Georgia, Michigan, Florida, Pennsylvania, Illinois, Tennessee, Virginia, Missouri, South Dakota, California, Montana, Minnesota, Arizona
Description
Insufficient weld around the cap component of the instrument is insufficient to withstand impaction forces.
Product
Brand Name: Meridian Angled Awl Fixed Product Name: Angled Awl Fixed Model/Catalog Number: RA2-003015 Product Description: Surgical Awl Component: No
Manufacturer(s)
SEASPINE ORTHOPEDICS CORPORATION
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →