Zimmer Biomet, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0709-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Biomet DVR Crosslock Screws- 2.7mm x18mm, Sterile ITEM 131827118 Product Usage: Usage: The system is intended for stabilization and fixation of small bone fragments in fresh fractures, revision procedures, joint fusion and reconstructions (osteotomies) of small bones of the hand, foot, radius, ulna, ankle, humerus, scapula and pelvis, particularly in osteopenic bone

Product Classification:

Class II

Date Initiated: November 20, 2018

Date Posted: January 16, 2019

Recall Number: Z-0709-2019

Event ID: 81704

Reason for Recall:

One lot of product labeled 2.7mm x18mm Lock Screw Square Drive (Lot 029970) contains 20mm locking screws and one lot of product labeled 2.7mm x 20mm Lock Screw Square Drive (Lot 029980) contains 18mm locking screws

Status: Terminated

Product Quantity: 50 pieces

Code Information:

LOT 029970 UDI (01)00880304535572(17)280501(10)029970

Distribution Pattern:

Country of Japan

Voluntary or Mandated:

Voluntary: Firm initiated