PediaLift recalls 12 units of Access Device (serial numbers PCL-HDPE-DL-1 to PCL-HDPE-DL-12) due to missing compliance certificate. No action needed as the hazard is non-operational.
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.
PediaLift is recalling 12 specific Access Devices because the original vendor did not provide a compliance certificate. This issue does not affect safety or function of the device.
The device lacks a required compliance certificate from the original vendor. This means the product may not meet labeling requirements, but it does not cause injury or malfunction.
Owners of the recalled Access Devices with serial numbers PCL-HDPE-DL-1 through PCL-HDPE-DL-12 are affected. No one is at risk of injury.
Check for serial numbers starting with PCL-HDPE-DL-1 to PCL-HDPE-DL-12 on the PediaLift Access Device. The device identifier is B751PDLFT0.
Look for serial numbers PCL-HDPE-DL-1 through PCL-HDPE-DL-12 on the device.
No, the device does not cause injury or malfunction. The issue is a missing compliance certificate, which does not affect safety.
No action is required as the hazard is non-operational and does not pose a risk.
Check for serial numbers PCL-HDPE-DL-1 through PCL-HDPE-DL-12 on the PediaLift Access Device.
We’ve drafted a message you can send PediaLift to request your refund or repair — edit it as you like.
Subject: Recall Z-0931-2020 — PediaLift PediaLift Hello, I own a PediaLift that is covered by recall Z-0931-2020 from PediaLift. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.