Class II — Potential Health Hazard

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...

Date: November 17, 2021
Company: Medshape, INC.
Status: Ongoing
Source: FDA (Device)

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

Affected (9 states)Not affected

About Medshape, INC.

Medshape, INC. has 2 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report