Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DYNANAIL MINI Recalled by Medshape, INC. Due to The firm identified a nonconformance in Lot 04882...
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 Medshape, INC. directly.
Affected Products
DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
Quantity: 26 units (1 count)
Why Was This Recalled?
The firm identified a nonconformance in Lot 04882 involving the endcap being manufactured to a longer length than indicated in product specifications, introducing the risk of the +6 mm endcap not seating flush with the nail while inserting during a procedure.
Where Was This Sold?
This product was distributed to 9 states: CA, FL, GA, IL, IN, MD, MA, TX, WA
About Medshape, INC.
Medshape, INC. 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