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H1952 HomeCare Standard Crib
HARD MANUFACTURING CO., INC. · Model H1952 · UDI-DI 00852231007705
FMS
Prescription
10
510(k) clearances
1,272
Adverse events (2 deaths)
5
Recalls
25
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-02-18 | Stryker Medical Division of Stryker Corporation | Cribs sold in the USA are missing two access door warning labels. |
| 2021-05-12 | Stryker Medical Division of Stryker Corporation | Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately iden |
| 2019-07-03 | PediaLift LLC | The firm was unsuccessful in obtaining a satisfactory Certificate of Conformance from the original vendor of the mattress showing that they are in compliance with labeling require |
| 2003-12-19 | Hill-Rom, Inc. | The caster/wheel may come off of the bassinet, causing the bassinet to tip. |
| 2003-12-19 | Hill-Rom, Inc. | The caster/wheel may come off of the bassinet, causing the bassinet to tip. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.