Medicrea International: Medical Device Recall in 2020 - (Recall #: Z-0828-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Medicrea Pass LP Blunt K-wire 01.6mm x 500mm-Nitinol Product reference: A06010140

Product Classification:

Class II

Date Initiated: September 16, 2019

Date Posted: January 29, 2020

Recall Number: Z-0828-2020

Event ID: 84595

Reason for Recall:

Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the minimum tolerance axis threaded

Status: Ongoing

Product Quantity: 190 units

Code Information:

Lot number(s) : 18G0368; 19H0009; 18F0138; 18G0038

Distribution Pattern:

Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated