Cub Pediatric Crib, Model FL19H
USCub Pediatric Crib, Model FL19H
Recalling Firm: Stryker Medical Division of Stryker Corporation
Grund für den Rückruf / Gefahr
TranslatedCribs sold in the USA are missing two access door warning labels.
Produktbeschreibung & Identifikation
TranslatedCub Pediatric Crib, Model FL19H
Additional Source Details
| Field | Value |
|---|---|
| City | Portage |
| State | MI |
| Event id | 98426 |
| Address 1 | 3800 E Centre Ave |
| Address 2 | N/A |
| Code info | 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... [TRUNCATED] |
| Postal code | 49002-5826 |
| Report date | 20260325 |
| Product type | Devices |
| Product quantity | 590 |
| Reason for recall | Cribs sold in the USA are missing two access door warning labels. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260218 |
| Initial firm notification | Letter |
| Center classification date | 20260319 |
Consumer Action Protocol: What You Should Do Immediately
Safety StepsInspect the NDC code, batch number, or control number on your medicine bottle or blister packaging to confirm whether your unit is included.
Do not abruptly stop critical prescribed medication without physician advice. Contact your dispensing pharmacist immediately for a safe alternative.
Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.
If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (FDA Devices).
Your Legal Rights as a Consumer
Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.
Frequently Asked Questions About This Recall
FAQ GuideQ1:What should I do immediately if I own or bought Cub Pediatric Crib, Model FL19H?
Check the lot number and NDC on your prescription label. For essential medications, consult your doctor or dispensing pharmacist immediately before abruptly stopping your dose.
Q2:Can I get a full refund or free repair for this recall?
Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.
Q3:Do I need my original sales receipt to claim a remedy or refund?
In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.
Q4:Where can I verify official information for this safety alert?
This safety alert is aggregated directly from official regulatory agency records (FDA Devices). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.
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Übersicht
- Rückrufendes UnternehmenStryker Medical Division of Stryker Corporation
- StatusOngoing
- RisikostufeClass II
- DistributionUS Nationwide distribution.
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🚨 SAFETY ALERT: Stryker Medical Division of Stryker Corporation - Cub Pediatric Crib, Model FL19H Check if your household is affected: https://therecallfile.com/de/recalls/cub-pediatric-crib-model-fl19h/FDA-Z-1580-2026
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