Recall Z-1580-2026— Stryker Medical Division of Stryker Corporation
Class II · Ongoing
Class II FDA medical device recall by Stryker Medical Division of Stryker Corporation, initiated 2026-02-18. FDA's recall record names no specific 510(k) clearance for this event. Product: Cub Pediatric Crib, Model FL19H. Reason: Cribs sold in the USA are missing two access door warning labels..
- Recalling firm
- Stryker Medical Division of Stryker Corporation
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-02-18
- Firm location
- Portage, MI, United States
Product description
Cub Pediatric Crib, Model FL19H
Reason for recall
Cribs sold in the USA are missing two access door warning labels.
Data sourced from openFDA. This site is unofficial and independent of the FDA.