Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Valeris Medical Apollo Medial Suture Anchor Recalled by Valeris Medical, LLC Due to Mislabeling
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 Valeris Medical, LLC directly.
Affected Products
Valeris Medical Apollo Medial Suture Anchor, Catalog Number MSA-4515, 4.5 x 15mm, each package contains (1) PEEK Screw, (1) #2 ForceBraid Blue, and (1) #2 ForceBraid White, 5 packages per container, Sterile, Rx. The firm name on the label is Valeris Medical, Marietta, GA.
Quantity: 75 units
Why Was This Recalled?
The product was mislabeled as containing the incorrect type of suture.
Where Was This Sold?
This product was distributed to 4 states: FL, OH, OK, TX
About Valeris Medical, LLC
Valeris Medical, LLC has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report