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PediaLift LLC recalls PediaLift Access Device, Device Identifier: B751PDLFT0
Recalled February 12, 2020 · FDA recall Z-0931-2020 · PediaLift
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. · FDA Class II
Units
11
Sold at
The products were distributed to the following US states: IN, NJ, NY, OH, and PA
Description
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.
Product
PediaLift Access Device, Device Identifier: B751PDLFT0
Manufacturer(s)
PediaLift LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →