Bed, Pediatric Open Hospital
FDA adverse event reports and recall history for bed, pediatric open hospital (product code FMS), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 1,269
- Deaths
- 2
- Injuries
- 36
- Malfunctions
- 1,193
Reports per year
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
- 2026-03-19Open, ClassifiedUnder Investigation by firm
Cub Pediatric Crib, Model FL19H
Cribs sold in the USA are missing two access door warning labels.
- 2004-01-08TerminatedOther
Hill-Rom Newborn bassinet; model P247.
The caster/wheel may come off of the bassinet, causing the bassinet to tip.
- 2004-01-08TerminatedOther
Hill-Rom Newborn bassinet; model P248.
The caster/wheel may come off of the bassinet, causing the bassinet to tip.
- TerminatedNonconforming Material/Component
PediaLift Access Device, Device Identifier: B751PDLFT0
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 requirements.
- Open, ClassifiedUnder Investigation by firm
CUB Pediatric Crib- intended to provide a pediatric patient support surface for medical purposes and to provide a method of transporting pediatric patients within a healthcare facility Model Number: FL19 Part #5050000000
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 identifies the correct use environment, but home users may not be aware of or fully understand these instructions intended for healthcare professionals
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