Mansfield, OH, United States
PediaLift LLC recalls
1 recall recorded since 2018, most recently on 3 July 2019. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 3 July 2019
- Terminated
- 15 May 2020
- Reason
- 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
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0931-2020
- PediaLift Access Device, Device Identifier: B751PDLFT0
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.