Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Brand Name: Meridian Angled Awl Fixed Product Name: Angled Awl Recalled by SEASPINE ORTHOPEDICS CORPORATION Due to Insufficient weld around the cap component of the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact SEASPINE ORTHOPEDICS CORPORATION directly.
Affected Products
Brand Name: Meridian Angled Awl Fixed Product Name: Angled Awl Fixed Model/Catalog Number: RA2-003015 Product Description: Surgical Awl Component: No
Quantity: 100 units
Why Was This Recalled?
Insufficient weld around the cap component of the instrument is insufficient to withstand impaction forces.
Where Was This Sold?
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
About SEASPINE ORTHOPEDICS CORPORATION
SEASPINE ORTHOPEDICS CORPORATION has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report