Biomet, Inc.: Medical Device Recall in 2020 - (Recall #: Z-0093-2021)

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:

Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate with Taper Adapter-Shoulder Prosthesis item: 010000589 - Product Usage: intended to serve as the foundation for the reverse shoulder prosthesis head (glenosphere).

Product Classification:

Class II

Date Initiated: September 2, 2020

Date Posted: October 21, 2020

Recall Number: Z-0093-2021

Event ID: 86422

Reason for Recall:

Product potentially being packaged without a taper adapter or baseplate. The package should contain one (1) baseplate and one (1) taper adapter, product may be packaged with two (2) baseplates and no (0) adapters or with no (0) baseplates and two (2) adapters

Status: Terminated

Product Quantity: 3 units

Code Information:

Lot Numbers: 488150 -UDI (01) 00880304532465 (17) 300623 (10) 488150; and 564110- UDI (01) 00880304532465 (17) 300609 (10) 564110

Distribution Pattern:

US Nationwide distribution including in the states of CO, MN, OH, WY.

Voluntary or Mandated:

Voluntary: Firm initiated