Crossroads Extremity Systems Llc: Medical Device Recall in 2017 - (Recall #: Z-1487-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

MotoCLIP(TM) Super Elastic Fusion System, Size 18mm x 14mm x 14mm, REF 1442-1814, Rx Only, STERILE R.

Product Classification:

Class II

Date Initiated: February 16, 2017

Date Posted: March 29, 2017

Recall Number: Z-1487-2017

Event ID: 76687

Reason for Recall:

Seven 18mm x 18mm x 18 mm implants had been placed in kits, packed and labeled as 18mm x 14mm x 14mm.

Status: Terminated

Product Quantity: 20 units

Code Information:

Lot Number 101868

Distribution Pattern:

Al, FL, IN, Il, NE, TX, NM, CO, AZ

Voluntary or Mandated:

Voluntary: Firm initiated