Biomet, Inc.: Medical Device Recall in 2020 - (Recall #: Z-1615-2020)

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-indicated for primary, fracture, or revision total shoulder replacement for the relief of pain and significant disability due to gross rotator cuff deficiency Item Number: 010000589

Product Classification:

Class II

Date Initiated: February 25, 2020

Date Posted: April 8, 2020

Recall Number: Z-1615-2020

Event ID: 85143

Reason for Recall:

Package is intended to contain one (1) baseplate and one (1) taper adapter; however, devices may be packaged with two (2) baseplates and no (0) adapters.

Status: Terminated

Product Quantity: 21 units

Code Information:

Lot Number: 410420 UDI: (01) 0 0880304 53246 5 (17) 290825 (10) 410420

Distribution Pattern:

International distribution - country of Netherland.s

Voluntary or Mandated:

Voluntary: Firm initiated