Class II
Medical Device Recall: Cub Pediatric Crib, Model FL19H
Stryker Medical Division of Stryker Corporation · February 18, 2026
Reason for Recall
Cribs sold in the USA are missing two access door warning labels.
Distribution
US Nationwide distribution.
States Affected
NATIONWIDE
Quantity Affected
590
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1580-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.