Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
AVE 2 Birthing Bed - Product Usage: is designated to Recalled by Linet Americas Due to The UDI on the device label indicates incorrect...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Linet Americas directly.
Affected Products
AVE 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.
Quantity: 202 devices
Why Was This Recalled?
The UDI on the device label indicates incorrect manufacturer.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Linet Americas
Linet Americas has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report