Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PediaLift Access Device Recalled by PediaLift LLC Due to The firm was unsuccessful in obtaining a satisfactory...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact PediaLift LLC directly.
Affected Products
PediaLift Access Device, Device Identifier: B751PDLFT0
Quantity: 11
Why Was This 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.
Where Was This Sold?
This product was distributed to 5 states: IN, NJ, NY, OH, PA
About PediaLift LLC
PediaLift LLC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report