Biomet, Inc.: Medical Device Recall in 2023 - (Recall #: Z-0384-2024)

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 Short Anchor Plug, 22 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178564

Product Classification:

Class II

Date Initiated: October 9, 2023

Date Posted: November 29, 2023

Recall Number: Z-0384-2024

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: 441020 (01)00880304461628(17)270915(10)441020; 535430 (01)00880304461628(17)270701(10)535430; 577560 (01)00880304461628(17)270725(10)577560; 577740 (01)00880304461628(17)271114(10)577740; 608760 (01)00880304461628(17)271112(10)608760; 671870 (01)00880304461628(17)280131(10)671870; 975160 (01)00880304461628(17)270806(10)975160

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated