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Open, Classified

Cub Pediatric Crib, Model FL19H

FDA Recall Z-1580-2026 · Posted 2026-03-19

Recalling FirmStryker Medical Division of Stryker Corporation
Recall StatusOpen, Classified
Product CodeFMS
Date Initiated2026-02-18
Product Quantity590

Reason for Recall

Cribs sold in the USA are missing two access door warning labels.

Firm Action

On February 18. 2026, the firm notified customers through IMPORTANT MEDICAL DEVICE CORRECTION letters. Customers were notified of the missing warning labels, which read, "WARNING: Never leave a child unsupervised when the movable slide is open or not secured Refer to Instructions for Use for product care, maintenance, and cleaning." Customers were instructed to locate the units listed on the attached business reply form and identify the address where they can be serviced, and return the completed form to Stryker. Stryker will then contact consignees to arrange for the application of the missing label. In the interim, until the service can be performed, all pertinent warnings and safety instructions may be found in the product manual: https://techweb.stryker.com/Stretcher/FL19/1607/Operations/1900-109- 001AC.0.pdf

Root Cause

Under Investigation by firm

Distribution Pattern

US Nationwide distribution.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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