Biomet, Inc.: Medical Device Recall in 2020 - (Recall #: Z-2300-2020)

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:

Comprehensive VRS Inserter, shoulder prosthesis, Item No. 110019068. UDI: (01)00880304829503 (10)814100, (01)00880304829503 (10)570640, (01)00880304829503 (10)728890, (01)00880304829503 (10)977300

Product Classification:

Class II

Date Initiated: May 11, 2020

Date Posted: June 17, 2020

Recall Number: Z-2300-2020

Event ID: 85658

Reason for Recall:

The product is being recalled due to the central screw drill seizing inside the Comprehensive VRS Inserter, which may lead to an extension of surgery to find a replacement device.

Status: Terminated

Product Quantity: 38

Code Information:

Lots 814100, 570640, 728890, 977300

Distribution Pattern:

US Nationwide Distribution in the states of CA, FL, IN, KS, KY, MI, OH, and TX. Foreign distribution to Netherlands.

Voluntary or Mandated:

Voluntary: Firm initiated