# FDA recall Z-0931-2020

> **PediaLift LLC** · Class II · device recall initiated 2019-07-03.

## Product

PediaLift Access Device, Device Identifier: B751PDLFT0

## Reason for recall

The firm was unsuccessful in obtaining a satisfactory Certificate of   Conformance from the original vendor of the mattress showing that they are in compliance with labeling requirements.

## Distribution

The products were distributed to the following US states:  IN, NJ, NY, OH, and PA

## Key facts

- **Recall number:** Z-0931-2020
- **Recalling firm:** PediaLift LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-07-03
- **Report date:** 2020-02-12
- **Termination date:** 2020-05-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mansfield, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0931-2020

## Citation

> AI Analytics. FDA recall Z-0931-2020. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-0931-2020. Source: US FDA. Licensed CC0.

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