Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ally Bone Screw - Product Usage:Bone Screws are indicated for Recalled by PROVIDENCE MEDICAL TECHNOLOGIES Due to There may be dimensional manufacturing error that represents...
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 PROVIDENCE MEDICAL TECHNOLOGIES directly.
Affected Products
Ally Bone Screw - Product Usage:Bone Screws are indicated for use in bone reconstruction, osteotomy, arthrodesis, joint fusion, fracture repair, and fracture fixation appropriate for the size of the device. Screws are intended for single use only. L Providence Medical Technology, Inc. 3875 Hopyard Road, Suite 300, Pleasanton, CA 94588, Rx Only.
Quantity: 208 units
Why Was This Recalled?
There may be dimensional manufacturing error that represents a potential safety risk to patients.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About PROVIDENCE MEDICAL TECHNOLOGIES
PROVIDENCE MEDICAL TECHNOLOGIES has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report