FDA Device recall Z-1580-2026
Cub Pediatric Crib, Model FL19H
- FDA Device
- Class II
- ongoing
- Published 2026-03-25
On 2026-03-25 the FDA classified a Class II recall of Cub Pediatric Crib, Model FL19H by Stryker Medical Division, citing cribs sold in the USA are missing two access door warning labels.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1580-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-02-18 |
| Published | 2026-03-25 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Stryker Medical Division |
| Distribution | US |
Product
Cub Pediatric Crib, Model FL19H
Reason
Cribs sold in the USA are missing two access door warning labels.
Identifiers
| code_info | UDI-DI (GTIN) 07613327169348 Serial Numbers F61948 F61875 F61710 F62449 F62450 F62451 F62452 F62047 F62048 F62498 F624…UDI-DI (GTIN) 07613327169348 Serial Numbers 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 F61657 F61658 F61659 F61660 F61661 F61662 F61663 F61664 F61665 F61666 F61667 F61668 F61669 F61670 F61671 F61672 F61673 F61674 F61675 F61676 F61677 F61678 F61679 F61680 F61681 F61682 F61683 F61684 F61685 F61686 F61687 F61688 F61889 F61890 F61891 F61892 F61893 F61698 F61699 F62448 F61972 F61988 F61989 F62181 F62501 F62502 F62532 F62533 F62432 F62446 F62447 F61595 F61992 F61993 F62125 F62389 F61894 F62123 F61742 F61743 F62117 F62118 F62119 F62433 F62434 F62435 F62436 F62437 F61917 F61918 F61919 F61920 F61921 F61922 F61923 F61924 F61925 F61926 F61927 F61928 F61929 F61930 F61865 F61866 F62159 F62160 F62 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1580-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.