PediaLift LLC recalls PediaLift Access Device, Device Identifier: B751PDLFT0
Recalled Product
PediaLift Access Device, Device Identifier: B751PDLFT0
Hazard / Issue
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.
Issued by
FDA
Affected States: IN, NJ, NY, OH, PA
Lot/Code Info: 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
View official government recall
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