FDAJanuary 7, 2019device
AVE 2 Birthing Bed
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
LINET has recently become aware of a potential safety issue for the AVE 2 Birthing Bed caused by the power cable breaking at the bed connection or the orange insulation of the power cable may fail causing a possible spark or possible exposure to a live conductor.
What to do
FDA enforcement status: Terminated
Brands named
linet spol s r olinetlinet spol
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDASprint 200 wheeled stretcher, Item numbers 1ES200-7, 1ES210-1, and 1ES211-1.2023-01-18
- FDAAVE 2 Birthing Bed - Product Usage: is designated to be used by mothers ready for spontaneous vaginal delivery and also as aid to search for individual positions providing relief in all delivery stages including postpartum period. Birthing bed is not intended for use as a general hospital bed.2020-03-06
- FDAEleganza 5 (AC powered adjustable bed), Item Numbers: a) 1GE512055-40, b) 1GE512055-45, c) 1GE512055-85, and d) 1GE512055-95 - Product Usage: Eleganza 5 is a positionable bed for intensive care. Its purpose is to support patient and to facilitate treatment and manipulation with patient for nursin...2019-11-13
Own something like this?
AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.
Start free — 200 items, no card →