Stanmore Implants Worldwide Ltd.: Medical Device Recall in 2016 - (Recall #: Z-1623-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Distal Femoral Replacement (patient specific, custom made orthopedic implant device). PIN 19960

Product Classification:

Class II

Date Initiated: April 12, 2016

Date Posted: May 18, 2016

Recall Number: Z-1623-2016

Event ID: 73856

Reason for Recall:

Incorrect component used to manufacture distal femoral replacement.

Status: Terminated

Product Quantity: 1

Code Information:

Device Identifier: PIN 19960, Lot: 19960

Distribution Pattern:

US distribution to OH.

Voluntary or Mandated:

Voluntary: Firm initiated