Biomet, Inc.: Medical Device Recall in 2020 - (Recall #: Z-0631-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

RingLoc+ Quick Connect Drill Bit, Item numbers 31-323215, 31-323220, 31-323230, 31-323240 - Product Usage: Bit, Drill.

Product Classification:

Class II

Date Initiated: November 25, 2020

Date Posted: December 23, 2020

Recall Number: Z-0631-2021

Event ID: 86896

Reason for Recall:

Specific lots of multiple sterile medical devices may have a breach in the sterile seal. A breach in the packaging seal could lead to loss of sterility of the device.

Status: Terminated

Product Quantity: 7428

Code Information:

Lots 492670 562350 253280 253290 253300 278210 278230 417030 608110 608150 677300 253320 267910 267920 267930 267940 267960 267970 278160 363700 363720 363740 386960 492750 507930 507940 507980 508000 232590 232610 386830 386850 386860 386870 492720 530950 386840

Distribution Pattern:

Worldwide distribution. US nationwide, ARGENTINA, AUSTRALIA, Brazil, CANADA, CHILE, CHINA, COSTA RICA, EMEA, HONG KONG, INDIA, JAPAN, KOREA, MALAYSIA, NEW ZEALAND, SINGAPORE, and TAIWAN

Voluntary or Mandated:

Voluntary: Firm initiated