Biomet, Inc.: Medical Device Recall in 2023 - (Recall #: Z-0374-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Compress Device Segmental Anchor Plug, 18 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178408

Product Classification:

Class II

Date Initiated: October 9, 2023

Date Posted: November 29, 2023

Recall Number: Z-0374-2024

Event ID: 93323

Reason for Recall:

Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery

Status: Ongoing

Product Quantity: N/A

Code Information:

Lot Numbers/UDI: 017910 (01)00880304259768(17)270807(10)017910; 017910R (01)00880304259768(17)270807(10)017910R; 018060 (01)00880304259768(17)270817(10)018060; 332060 (01)00880304259768(17)270817(10)332060; 608610 (01)00880304259768(17)271204(10)608610; 671740 (01)00880304259768(17)271117(10)671740; 671740R (01)00880304259768(17)271117(10)671740R; 752790 (01)00880304259768(17)270816(10)752790; 752790R (01)00880304259768(17)270816(10)752790R; 965290 (01)00880304259768(17)271030(10)965290;

Distribution Pattern:

Worldwide distribution - US Nationwide and the countries of ARGENTINA, AUSTRALIA, CANADA, CHILE, JAPAN, NETHERLANDS, NEW ZEALAND.

Voluntary or Mandated:

Voluntary: Firm initiated