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.

Stryker Medical Division of Stryker Corporation Medical Device Recall: Cub Pediatric Crib, Model FL19H | SafeCheck