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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Baby & Nursery/Cribs & Bassinets

Cub Pediatric Cribs Recalled for Missing Access Door Warning Labels

Agency Publication Date: March 19, 2026
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Summary

Stryker Medical is recalling 590 Cub Pediatric Cribs (Model FL19H) because they are missing two required safety warning labels on the access doors. Without these labels, users may not be aware of critical safety instructions for operating the crib doors. These units were distributed across the United States between February and March 2026.

Risk

The missing warning labels could lead to improper use of the crib's access doors, potentially increasing the risk of entrapment or falls for pediatric patients. No injuries or incidents have been reported to date.

What You Should Do

  1. Identify your device by checking the model number FL19H and the serial number on the product label.
  2. Check the serial number against the list of 590 affected units. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.
  4. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) if you have further questions or need to report an issue.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Cub Pediatric Crib
Model / REF:
FL19H
Serial Numbers (589):
F61948
F61875
F61710
F62449
F62450
F62451
F62452
F62047
F62048
F62498
F62499
F62500
F61619
F61620
F61621
F61622
F61623
F61624
F61625
F61626
F61627
F61628
F61629
F61630
F61631
F61632
F61633
F61634
F61635
F61636
F61637
F61638
F61639
F61640
F61641
F61642
F61643
F61644
F61645
F61646
F61647
F61648
F61649
F61650
F61651
F61652
F61653
F61654
F61655
F61656
UDI:
07613327169348
GTIN:
07613327169348

Units missing two access door warning labels.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98426
Status: Active
Manufacturer: Stryker Medical Division of Stryker Corporation
Sold By: Authorized Medical Distributors; Stryker Direct Sales
Manufactured In: United States
Units Affected: 590
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.