PediaLift LLC recalls PediaLift Access Device, Device Identifier: B751PDLFT0

Recall date

July 3, 2019

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0931-2020

FDA classification

Class II

Brand / firm

PediaLift LLC

Sold / distributed

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

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

PediaLift Access Device, Device Identifier: B751PDLFT0