# FDA recall Z-2781-2020

> **Linet Americas** · Class III · device recall initiated 2020-03-06.

## Product

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.

## Reason for recall

The UDI on the device label indicates incorrect manufacturer.

## Distribution

US Nationwide distribution including in the states of Arkansas, California, Delaware, Florida, Georgia, Indiana, Louisiana, Massachusetts, Minnesota, Mississippi, Missouri, New Jersey, Oklahoma, Pennsylvania, Tennessee, Texas, West Virginia and Puerto Rico.

## Key facts

- **Recall number:** Z-2781-2020
- **Recalling firm:** Linet Americas
- **Classification:** Class III
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2020-03-06
- **Report date:** 2020-08-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Charlotte, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2781-2020

## Citation

> AI Analytics. FDA recall Z-2781-2020. Retrieved 2026-07-19 from https://api.ai-analytics.org/recall/Z-2781-2020. Source: US FDA. Licensed CC0.

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