Reported Feb 12, 2020 · Terminated
PediaLift Access Device, Device Identifier: B751PDLFT0
PediaLift LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: PediaLift LLC · 181 Illinois Ave S · Mansfield, OH · 44905-2825
Is this the product you have?
- PediaLift Access Device
- Device IdentifierB751PDLFT0
- Lot codes and dates
- Serial Numbers
PCL-HDPE-DL-1PCL-HDPE-DL-2PCL-HDPE-DL-3PCL-HDPE-DL-4PCL-HDPE-DL-5PCL-HDPE-DL-6PCL-HDPE-DL-7PCL-HDPE-DL-8PCL-HDPE-DL-9PCL-HDPE-DL-10PCL-HDPE-DL-11PCL-HDPE-DL-12
- Serial Numbers
- Amount recalled
- 11
Where it was sold
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.
This product could cause temporary or reversible health problems — stop using it.
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