Recall Z-0931-2020— PediaLift LLC
Class II · Terminated
Class II FDA medical device recall by PediaLift LLC, initiated 2019-07-03, terminated 2020-05-15. FDA's recall record names no specific 510(k) clearance for this event. Product: PediaLift Access Device, Device Identifier: B751PDLFT0. Reason: 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..
- Recalling firm
- PediaLift LLC
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-07-03
- Terminated
- 2020-05-15
- Firm location
- Mansfield, OH, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.