Product Wiki · Recalls · U.S. FDA — Device Enforcement

Cub Pediatric Crib, Model FL19H — recall Z-1580-2026

U.S. FDA — Device Enforcement · United States · 2026-02-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1580-2026
Date of alert
2026-02-18
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Stryker Medical Division of Stryker Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
07613327169348
Reported risk: Cribs sold in the USA are missing two access door warning labels.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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