PediaLift Access Device — Class II medical device recall Z-0931-2020
Terminated recall by PediaLift LLC, reported 2020-02-12, distributed in IN, NJ, NY, OH, PA. The firm was unsuccessful in obtaining a satisfactory Certificate of Conformance from the original vendor of t
| Recall number | Z-0931-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | PediaLift LLC, Mansfield, OH, United States |
| Recall initiated | 2019-07-03 |
| Classified | 2020-02-01 |
| Reported by FDA | 2020-02-12 |
| Terminated | 2020-05-15 |
| Distributed | IN, NJ, NY, OH, PA |
| Quantity | 11 |
| Reason classes | labeling |
| Serial numbers | PCL-HDPE-DL-1, PCL-HDPE-DL-10, PCL-HDPE-DL-11, PCL-HDPE-DL-12, 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 |
Product
PediaLift Access Device, Device Identifier: B751PDLFT0
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0931-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.