FDA recall, , Moderate risk
Stryker Cub Pediatric Crib
The Cub Pediatric Crib is missing two access door warning labels.
Summary by Recall Canary from the FDA notice
What happened
Stryker Medical Division of Stryker Corporation, located in Portage, Michigan, began a recall of the Cub Pediatric Crib, Model FL19H, on February 18, 2026, because cribs sold in the USA are missing two access door warning labels. The recall was added to the FDA's Enforcement Report on March 19, 2026, and was in the FDA's weekly enforcement report on March 25, 2026. The product was distributed nationwide in the US.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is your crib affected?
Match the model number and UDI-DI listed under your product.
A UDI-DI is the device identifier printed with the barcode on the device label.
Cub Pediatric Crib
- Model number
- FL19H
- UDI-DI
- 07613327169348
Recall details
- Company began the recall
- Sold in
US Nationwide distribution.
- Company
- Stryker Medical Division of Stryker CorporationPortage, Michigan
- Hazard
- Labeling error
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98426
- Recall number
- Z-1580-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
Summary updated
