Stryker Spine: Medical Device Recall in 2021 - (Recall #: Z-2100-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Cortoss Bone Augmentation Material 5cc Cartridge, Catalog Number 2101-0005, GTIN 00808232000962

Product Classification:

Class II

Date Initiated: May 18, 2021

Date Posted: July 28, 2021

Recall Number: Z-2100-2021

Event ID: 88217

Reason for Recall:

The products experienced a 12-hour excursion from the required refrigerated temperature conditions at the distribution center prior to distribution.

Status: Terminated

Product Quantity: 559 total

Code Information:

lot A1908003

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated