ClearanceBrief
Recall Z-1491-2025 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

Stryker Spine

Monterey AL Implant Inserter; 22mm; Catalog 48019140.

DateMar 31, 2025 (initiated Feb 28, 2025)
StatusOpen, Classified
ReasonPotential for the gold unlock button to separate from the inserter.
Root causeDevice Design
ActionOn February 28, 2025 URGENT MEDICAL DEVICE RECALL letters to inventory contacts. Actions needed 1. Immediately review the Product Recall Notification. Please forward this information to all sales representatives and operations teams within your Branch/Agency. Maintain awareness of this communication internally until all required actions have been completed within your facility. 2. Immediately check your internal inventory to locate the product listed on the attached Business Reply Form and remove them from their point of use. Note: Only Monterey AL Inserters with the lot number specified in th
Quantity44 units (41 US, 3 OUS)
DistributionDomestic: CA, CO, FL, GA, IL, MA, NE, NH, NY, OK, PA, TX, UT. International: Canada.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K201585Monterey AL Interbody System
Stryker Corporation, Aug 10, 2020