Zimmer Biomet, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0590-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Orthopedic Salvage System (OSS) Porous Stem, Item No. 150394

Product Classification:

Class II

Date Initiated: October 10, 2018

Date Posted: December 19, 2018

Recall Number: Z-0590-2019

Event ID: 81528

Reason for Recall:

Zimmer Biomet is conducting a lot specific medical device recall for two lots of the Orthopedic Salvage System (OSS) and the Comprehensive Shoulder System. The investigation determined that the Mini Humeral Stem is potentially labeled as the Bowed IM Stem lot. The associated risk of this product issue is a potential extension of surgery <30 minutes if a replacement is readily available.

Status: Terminated

Product Quantity: 3 total

Code Information:

068390

Distribution Pattern:

Distributed to accounts in IN, MD, MO, MS, and NM.

Voluntary or Mandated:

Voluntary: Firm initiated