FDA-Device2020-02-12Class II
PediaLift Access Device, Device Identifier: B751PDLFT0
PediaLift LLC
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.
Sold states
The products were distributed to the following US states: IN, NJ, NY, OH, and PA
Affected count
11
Manufactured in
181 Illinois Ave S, N/A, Mansfield, OH, United States
Products
PediaLift Access Device, Device Identifier: B751PDLFT0
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0931-2020Don't want to check this manually?
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