Medical DeviceAug 19, 2020
Linet Americas AVE 2 Birthing Bed - Product Usage: is designated to be used by mothers ready recall — FDA Z-2781-2020
The UDI on the device label indicates incorrect manufacturer.
Class IIIFDA: OngoingLinet Americas
Recall history in this database
Classification mix: Class III: 1.
Understanding this recall history
This page summarizes recall records in which the official source identifies Linet Americas as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.