Stryker Cub Pediatric Crib Model FL19H Missing Warning Labels
Stryker recalls Cub Pediatric Crib Model FL19H in the USA for missing two access door warning labels. This could lead to safety risks if the labels are needed for proper use.
Lower-risk recall
Cribs sold in the USA are missing two access door warning labels.
Contact the company
What happened, in plain English
Stryker is recalling Cub Pediatric Crib Model FL19H because they are missing two access door warning labels. This could be a safety risk if the labels are needed for proper use. Read more at govinfonow.com/recall/49963-stryker-cub-pediatric-crib-model-fl19h-missing-warning-labels.
Source Summary by GovInfoNow · govinfonow.com/recall/49963-stryker-cub-pediatric-crib-model-fl19h-missing-warning-labels · Updated August 17, 2026 · FDA enforcement record: FDA #Z-1580-2026
Cite this page
“Stryker Cub Pediatric Crib Model FL19H Missing Warning Labels.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/49963-stryker-cub-pediatric-crib-model-fl19h-missing-warning-labels. Based on FDA recall #Z-1580-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1580-2026%22&limit=1).
Why it’s dangerous
The crib is missing two access door warning labels that are necessary for safe use. Without these labels, users may not be aware of proper safety procedures for accessing the crib.
Who’s affected
Parents or caregivers who own or use the Cub Pediatric Crib Model FL19H in the USA are likely affected. Children using this crib are at the highest risk.
How to tell if you have this one
Check for the Cub Pediatric Crib Model FL19H with serial numbers listed in the recall notice. The product was sold in the USA and has specific serial numbers provided in the recall.
- Brand
Stryker- Category
Medical device
What to do — step by step
Check Crib Labels
Look for the two missing access door warning labels on the crib. If they are missing, the crib is part of the recall.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 35 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Similar recalls
Latest medical device recalls
Keep exploring
Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-1580-2026 (February 18, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1580-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.