FDA recall Z-0931-2020

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

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

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