Biomet, Inc.: Medical Device Recall in 2023 - (Recall #: Z-0372-2024)

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, 14 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178404

Product Classification:

Class II

Date Initiated: October 9, 2023

Date Posted: November 29, 2023

Recall Number: Z-0372-2024

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 017900 (01)00880304002890(17)270912(10)017900; 017900R (01)00880304002890(17)270912(10)017900R; 240760 (01)00880304002890(17)270120(10)240760; 332020 (01)00880304002890(17)270725(10)332020; 332040 (01)00880304002890(17)270629(10)332040; 608500 (01)00880304002890(17)270830(10)608500; 608590 (01)00880304002890(17)271030(10)608590; 609150 (01)00880304002890(17)270830(10)609150; 671670 (01)00880304002890(17)271030(10)671670; 712220 (01)00880304002890(17)270114(10)712220; 752770 (01)00880304002890(17)270814(10)752770; 798020 (01)0 0880304002890(17)270120(10)798020; 965310 (01)00880304002890(17)271112(10)965310,

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated