PediaLift LLC: Medical Device Recall in 2020 - (Recall #: Z-0931-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

PediaLift Access Device, Device Identifier: B751PDLFT0

Product Classification:

Class II

Date Initiated: July 3, 2019

Date Posted: February 12, 2020

Recall Number: Z-0931-2020

Event ID: 84591

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.

Status: Terminated

Product Quantity: 11

Code Information:

Serial Numbers: PCL-HDPE-DL-1, PCL-HDPE-DL-2, PCL-HDPE-DL-3, PCL-HDPE-DL-4, PCL-HDPE-DL-5, PCL-HDPE-DL-6, PCL-HDPE-DL-7, PCL-HDPE-DL-8, PCL-HDPE-DL-9, PCL-HDPE-DL-10, PCL-HDPE-DL-11, PCL-HDPE-DL-12

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated