Cub Pediatric Crib — Class II medical device recall Z-1580-2026
Ongoing recall by Stryker Medical Division of Stryker Corporation, reported 2026-03-25, distributed nationwide. Cribs sold in the USA are missing two access door warning labels.
| Recall number | Z-1580-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Medical Division of Stryker Corporation, Portage, MI, United States |
| Recall initiated | 2026-02-18 |
| Classified | 2026-03-19 |
| Reported by FDA | 2026-03-25 |
| Distributed | Nationwide (US) |
| Quantity | 590 |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 07613327169348 |
| Serial numbers | F61447, F61449, F61450, F61570, F61571, F61572, F61573, F61574, F61575, F61576, F61577, F61579, F61580, F61581, F61582, F61583, F61584, F61585, F61589, F61590, F61592, F61593, F61595, F61604, F61605 and 475 more |
| Model numbers | FL19H |
Product
Cub Pediatric Crib, Model FL19H
Reason for recall
Cribs sold in the USA are missing two access door warning labels.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1580-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.