Medshape, INC.: Medical Device Recall in 2022 - (Recall #: Z-0453-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile

Product Classification:

Class II

Date Initiated: November 17, 2021

Date Posted: January 12, 2022

Recall Number: Z-0453-2022

Event ID: 89117

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 26 units (1 count)

Code Information:

Model No. 2600-05-006; Lot No. 04882; UDI: M97026000500060

Distribution Pattern:

Domestic: CA, FL, GA, IL, IN, MA, MD, TX, and WA.

Voluntary or Mandated:

Voluntary: Firm initiated