# FDA recall Z-0991-2019

> **Linet Spol. S.r.o.** · Class II · device recall initiated 2019-01-07.

## Product

AVE 2 Birthing Bed

## Reason for recall

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.

## Distribution

AL, OK, NJ, OR, WA, CA, MN, LA, AZ, IL, MO, CO, OH, KY, FL, KS, UT, TN, LA, DE, CT, TX

## Key facts

- **Recall number:** Z-0991-2019
- **Recalling firm:** Linet Spol. S.r.o.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-01-07
- **Report date:** 2019-03-20
- **Termination date:** 2023-05-31

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Slany, N/A, Czech Republic

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0991-2019

## Citation

> AI Analytics. FDA recall Z-0991-2019. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/Z-0991-2019. Source: US FDA. Licensed CC0.

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