Synthes (USA) Products LLC: Medical Device Recall in 2013 - (Recall #: Z-0406-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Synthes 2.4 mm LC-DCP Plate 6 Holes/51mm Product Usage: Intended for fractures, osteotomies, and replantations of small bones including the foot, ankle, and hand.

Product Classification:

Class II

Date Initiated: July 30, 2013

Date Posted: December 4, 2013

Recall Number: Z-0406-2014

Event ID: 66413

Reason for Recall:

A complaint was reported regarding a screw being found in a package labeled for 2.4 mm LC-DCP Plate.

Status: Terminated

Product Quantity: 13

Code Information:

Part No. 249.926, lot No. 8093100

Distribution Pattern:

Worldwide Distribution - USA (nationwide) including IN, NY, WA, NE, MD, TX, AL, MI, and Internationally to Canada.

Voluntary or Mandated:

Voluntary: Firm initiated