FDAJuly 3, 2019device
PediaLift Access Device, Device Identifier: B751PDLFT0
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
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.
What to do
FDA enforcement status: Terminated
Brands named
pedialift
Recall history
No related federal recalls on record for this brand yet.
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